SLC10A1, solute carrier family 10 member 1, 6554

N. diseases: 54; N. variants: 7
Disease: Complete atrioventricular block ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2296651
rs2296651
Entrez Id: 6554
Gene Symbol: SLC10A1
SLC10A1
CUI: C0151517
Disease:
Complete atrioventricular block 		0.040 GeneticVariation BEFREE Intriguingly, ten individuals were identified as S267F homozygotes in population studies of chronic hepatitis B (CHB) patients. 30032030 2018
dbSNP: rs2296651
rs2296651
Entrez Id: 6554
Gene Symbol: SLC10A1
SLC10A1
CUI: C0151517
Disease:
Complete atrioventricular block 		0.040 GeneticVariation BEFREE The frequency of the S267F variant in CHB, cirrhosis and hepatocellular carcinoma (HCC) patients was 3.3%, 0.9%, and 3.5%, respectively. 29247233 2017
dbSNP: rs2296651
rs2296651
Entrez Id: 6554
Gene Symbol: SLC10A1
SLC10A1
CUI: C0151517
Disease:
Complete atrioventricular block 		0.040 GeneticVariation BEFREE The frequency of rs2296651-GA was inversely correlated with CHB, LC or HCC patients [adjusted OR(95%CI)=0.16(0.11-0.23), <i>p</i><0.001; 0.34(0.21-0.55), <i>p</i>=0.001; or 0.46(0.25-0.83), <i>p</i>=0.008], respectively, compared with HCs. 29285260 2017
dbSNP: rs2296651
rs2296651
Entrez Id: 6554
Gene Symbol: SLC10A1
SLC10A1
CUI: C0151517
Disease:
Complete atrioventricular block 		0.040 GeneticVariation BEFREE Together with serum HBV DNA levels, S267F may help to identify patients with CHB with very low risk of HCC. 26642861 2016