AS3MT, arsenite methyltransferase, 57412

N. diseases: 56; N. variants: 18
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10748835
rs10748835
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0023487
Disease:
Acute Promyelocytic Leukemia
0.010 GeneticVariation BEFREE Our data promotes the realization that AS3MT 35587 (rs11191453), 35991 (rs10748835), especially their joint genotypes 35991 (rs10748835) AA / 35587 (rs11191453) TC+CC, is a novel predictive biomarker for the therapeutic efficacy of As<sub>2</sub>O<sub>3</sub> in the treatment of APL. 31330140 2019
dbSNP: rs11191439
rs11191439
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0023487
Disease:
Acute Promyelocytic Leukemia
0.010 GeneticVariation BEFREE In this article, the associations among urinary arsenic profiles, hematological and biochemical values, and 3 AS3MT genotypes (rs3740392, rs3740390, and rs11191439) were evaluated in 50 APL patients treated with arsenic trioxide (As2O3). 30376134 2018
dbSNP: rs11191453
rs11191453
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0023487
Disease:
Acute Promyelocytic Leukemia
0.010 GeneticVariation BEFREE Our data promotes the realization that AS3MT 35587 (rs11191453), 35991 (rs10748835), especially their joint genotypes 35991 (rs10748835) AA / 35587 (rs11191453) TC+CC, is a novel predictive biomarker for the therapeutic efficacy of As<sub>2</sub>O<sub>3</sub> in the treatment of APL. 31330140 2019
dbSNP: rs3740390
rs3740390
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0023487
Disease:
Acute Promyelocytic Leukemia
0.010 GeneticVariation BEFREE These results indicate that inherent genetic information of the AS3MT rs3740390 genotypes is a novel predicted or evaluated target for As2O3-induced side effects and therapeutic efficacy for the treatment of APL. 30376134 2018
dbSNP: rs7909591
rs7909591
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0001948
Disease:
Alcohol consumption
T 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs12765002
rs12765002
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0003467
Disease:
Anxiety
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs3740393
rs3740393
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0003467
Disease:
Anxiety
C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs11191454
rs11191454
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.810 GeneticVariation BEFREE Our results provide preliminary evidence for the overtransmission of the A allele at the AS3MT rs11191454 polymorphism in ADHD. 25461954 2015
dbSNP: rs11191454
rs11191454
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.810 GeneticVariation GWASDB Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs11191454
rs11191454
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.810 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs11191454
rs11191454
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0004352
Disease:
Autistic Disorder
0.010 GeneticVariation BEFREE Therefore, this family-based association study was performed in 640 Chinese Han autism trios to investigate the association between autism and 7 SNPs with genome-wide significance in previous GWAS (rs4307059 near MSNP1AS, rs4141463 in MACROD2, rs2535629 in ITIH3, rs11191454 in AS3MT, rs1625579 in MIR137HG, rs11191580 in NT5C2, and rs1409313 in CUEDC2). 30610940 2019
dbSNP: rs11191454
rs11191454
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0005586
Disease:
Bipolar Disorder
0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs1046778
rs1046778
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0005695
Disease:
Bladder Neoplasm
0.020 GeneticVariation BEFREE The polymorphisms of AS3MT rs11191438, AS3MT rs10748835, and AS3MT rs1046778 were related to the risk of BC and UTUC, while the polymorphisms of AS3MT rs3740393, AS3MT rs11191453, and AS3MT rs11191454 were associated with arsenic methylation capacity. 29859237 2018
dbSNP: rs1046778
rs1046778
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0005695
Disease:
Bladder Neoplasm
0.020 GeneticVariation BEFREE High MMA%, low DMA% and AS3MT rs1046778 C/C + C/T genotype predicted a significantly higher risk of BC according to stepwise multiple logistic regression analyses. 29669044 2018
dbSNP: rs10748835
rs10748835
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0005695
Disease:
Bladder Neoplasm
0.020 GeneticVariation BEFREE The polymorphisms of AS3MT rs11191438, AS3MT rs10748835, and AS3MT rs1046778 were related to the risk of BC and UTUC, while the polymorphisms of AS3MT rs3740393, AS3MT rs11191453, and AS3MT rs11191454 were associated with arsenic methylation capacity. 29859237 2018
dbSNP: rs10748835
rs10748835
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0005695
Disease:
Bladder Neoplasm
0.020 GeneticVariation BEFREE The combination of AS3MT haplotype 2 (AS3MT rs11191453, rs11191454, rs10748835, and rs1046778)'s high-risk haplotype (C-G-A-C, T-A-A-C, and T-G-G-T) was significantly associated with increased risk of BC. 29669044 2018
dbSNP: rs11191438
rs11191438
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0005695
Disease:
Bladder Neoplasm
0.010 GeneticVariation BEFREE AS3MT rs11191438 (C > G) G/G genotype, AS3MT rs10748835 (A > G) G/G genotype, and AS3MT rs1046778 (C > T) T/T genotype were found to be related to BC risk, where the odds ratio (OR) (95% CI) was 0.50 (0.31-0.82), 0.49 (0.30-0.79), and 0.54 (0.36-0.80), respectively. 29669044 2018
dbSNP: rs11191439
rs11191439
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0005695
Disease:
Bladder Neoplasm
0.010 GeneticVariation BEFREE Individuals with one or more copies of the C allele in rs11191439 (the Met287Thr polymorphism) had an elevated risk of bladder cancer (OR = 1.17; 95% CI = 1.04-1.32 per 1 μg/L increase in average exposure). 22747749 2012
dbSNP: rs11191439
rs11191439
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0005695
Disease:
Bladder Neoplasm
0.010 GeneticVariation BEFREE Individuals with one or more copies of the C allele in rs11191439 (the Met287Thr polymorphism) had an elevated risk of bladder cancer (OR = 1.17; 95% CI = 1.04-1.32 per 1 μg/L increase in average exposure). 22747749 2012
dbSNP: rs11191454
rs11191454
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0005695
Disease:
Bladder Neoplasm
0.010 GeneticVariation BEFREE The polymorphisms of AS3MT rs11191438, AS3MT rs10748835, and AS3MT rs1046778 were related to the risk of BC and UTUC, while the polymorphisms of AS3MT rs3740393, AS3MT rs11191453, and AS3MT rs11191454 were associated with arsenic methylation capacity. 29859237 2018
dbSNP: rs3740393
rs3740393
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0005695
Disease:
Bladder Neoplasm
0.010 GeneticVariation BEFREE The polymorphisms of AS3MT rs11191438, AS3MT rs10748835, and AS3MT rs1046778 were related to the risk of BC and UTUC, while the polymorphisms of AS3MT rs3740393, AS3MT rs11191453, and AS3MT rs11191454 were associated with arsenic methylation capacity. 29859237 2018
dbSNP: rs12416687
rs12416687
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0005823
Disease:
Blood Pressure
T 0.700 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895 2014
dbSNP: rs72841270
rs72841270
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12765002
rs12765002
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs77335224
rs77335224
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C1305855
Disease:
Body mass index
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019