Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13231367
rs13231367
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0005612
Disease:
Birth Weight
G 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs13246286
rs13246286
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs150626020
rs150626020
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
T 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs325442
rs325442
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs35154268
rs35154268
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs6467157
rs6467157
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0005612
Disease:
Birth Weight
T 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs117123883
rs117123883
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs12536253
rs12536253
Entrez Id: 27044;105375492
Gene Symbol: SND1;LOC105375492
SND1;LOC105375492
CUI: C0021704
Disease:
Intelligence
C 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs3735634
rs3735634
Entrez Id: 27044;64101
Gene Symbol: SND1;LRRC4
SND1;LRRC4
CUI: C0596887
Disease:
mathematical ability
G 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs3735634
rs3735634
Entrez Id: 27044;64101
Gene Symbol: SND1;LRRC4
SND1;LRRC4
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs3757771
rs3757771
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs3808093
rs3808093
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs4731392
rs4731392
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs73234901
rs73234901
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs77999825
rs77999825
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs78066960
rs78066960
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs118049207
rs118049207
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Stratification and interaction analyses showed that SND1 rs118049207</span> multiplicatively interacted with the sex and drinking status of the patients to enhance their colorectal cancer risk (P = 1.56×10-3 and 1.41×10-2, respectively). 31579913 2020
dbSNP: rs118049207
rs118049207
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE Stratification and interaction analyses showed that SND1 rs118049207</span> multiplicatively interacted with the sex and drinking status of the patients to enhance their colorectal cancer risk (P = 1.56×10-3 and 1.41×10-2, respectively). 31579913 2020
dbSNP: rs3757769
rs3757769
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0153381
Disease:
Malignant neoplasm of mouth
0.010 GeneticVariation BEFREE We observed five SNPs-rs2051526 (ETV6), rs6021247 (NFATC2), rs3757769 (SND1), rs7085532 (TCF7L2), and rs7778413 (SND1) indicating increased oral cancer risk with OR ranging from 1.61 to 34.60. 31452252 2020
dbSNP: rs3757769
rs3757769
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0220641
Disease:
Lip and Oral Cavity Carcinoma
0.010 GeneticVariation BEFREE We observed five SNPs-rs2051526 (ETV6), rs6021247 (NFATC2), rs3757769 (SND1), rs7085532 (TCF7L2), and rs7778413 (SND1) indicating increased oral cancer risk with OR ranging from 1.61 to 34.60. 31452252 2020
dbSNP: rs7778413
rs7778413
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0153381
Disease:
Malignant neoplasm of mouth
0.010 GeneticVariation BEFREE We observed five SNPs-rs2051526 (ETV6), rs6021247 (NFATC2), rs3757769 (SND1), rs7085532 (TCF7L2), and rs7778413 (SND1) indicating increased oral cancer risk with OR ranging from 1.61 to 34.60. 31452252 2020
dbSNP: rs7778413
rs7778413
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0220641
Disease:
Lip and Oral Cavity Carcinoma
0.010 GeneticVariation BEFREE We observed five SNPs-rs2051526 (ETV6), rs6021247 (NFATC2), rs3757769 (SND1), rs7085532 (TCF7L2), and rs7778413 (SND1) indicating increased oral cancer risk with OR ranging from 1.61 to 34.60. 31452252 2020
dbSNP: rs778264641
rs778264641
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0521158
Disease:
Recurrent tumor
0.010 GeneticVariation BEFREE However, we identified a co-occurring somatic HRAS (p.Q61R) activating point mutation and MEN1 frameshift mutation (p.L117fs) present in a primary and recurrent tumor from one patient. 27175596 2016
dbSNP: rs17676986
rs17676986
Entrez Id: 27044;27099;105375492
Gene Symbol: SND1;SND1-IT1;LOC105375492
SND1;SND1-IT1;LOC105375492
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia
0.010 GeneticVariation BEFREE We found nine statistically significant associations with CLL risk after FDR correction, seven in miRNA processing genes (rs3805500 and rs6877842 in DROSHA, rs1057035 in DICER1, rs17676986 in SND1, rs9611280 in TNRC6B, rs784567 in TRBP and rs11866002 in CNOT1) and two in pre-miRNAs (rs11614913 in miR196a2 and rs2114358 in miR1206). 25793711 2015
dbSNP: rs1881084
rs1881084
Entrez Id: 27044
Gene Symbol: SND1
SND1
CUI: C0004352
Disease:
Autistic Disorder
0.010 GeneticVariation BEFREE Association analysis showed significant associations in MKL2 with ASD (rs756472, P=4.31 x 10(-5)) and between SND1 and strict autism (rs1881084, P=7.76 x 10(-5)) in the Finnish and Northern Dutch populations, respectively. 20442744 2010