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: rs7085104
rs7085104
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0036341
Disease:
Schizophrenia
A 0.800 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs12244388
rs12244388
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. 31268507 2019
dbSNP: rs12764899
rs12764899
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs12764899
rs12764899
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12764899
rs12764899
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0427460
Disease:
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12764899
rs12764899
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 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: 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: 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
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: 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: 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: 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: rs3740390
rs3740390
Entrez Id: 57412;100528007
Gene Symbol: AS3MT;BORCS7-ASMT
AS3MT;BORCS7-ASMT
CUI: C1956346
Disease:
Coronary Artery Disease
T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 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: 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: rs7909591
rs7909591
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0871470
Disease:
Systolic Pressure
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: rs1046778
rs1046778
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0699885
Disease:
Carcinoma of bladder
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: C0005684
Disease:
Malignant neoplasm of urinary bladder
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: C0005684
Disease:
Malignant neoplasm of urinary bladder
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: rs1046778
rs1046778
Entrez Id: 57412;100528007;107984265
Gene Symbol: AS3MT;BORCS7-ASMT;LOC107984265
AS3MT;BORCS7-ASMT;LOC107984265
CUI: C0699885
Disease:
Carcinoma of bladder
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: 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: C0005684
Disease:
Malignant neoplasm of urinary bladder
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: 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