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rs515726137

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs515726137(A;A)
Make rs515726137(A;C)
ReferenceGRCh38 38.1/142
Chromosome18
Position57669422
GeneATP8B1, RP11-35G9.3
is asnp
is mentioned by
dbSNPrs515726137
ebirs515726137
HLIrs515726137
Exacrs515726137
Varsomers515726137
Maprs515726137
PheGenIrs515726137
hapmaprs515726137
1000 genomesrs515726137
hgdprs515726137
ensemblrs515726137
gopubmedrs515726137
geneviewrs515726137
scholarrs515726137
googlers515726137
pharmgkbrs515726137
gwascentralrs515726137
openSNPrs515726137
23andMers515726137
23andMe allrs515726137
SNP Nexus

SNPshotrs515726137
SNPdbers515726137
MSV3drs515726137
GWAS Ctlgrs515726137
Max Magnitude0
ClinVar
Risk rs515726137(A;A)
Alt rs515726137(A;A)
Reference rs515726137(C;C)
Significance Pathogenic
Disease Progressive intrahepatic cholestasis
Variation info
Gene ATP8B1 LOC100505549
CLNDBN Progressive intrahepatic cholestasis
Reversed 0
HGVS NC_000018.9:g.55336654C>A
CLNSRC ClinVar
CLNACC RCV000114321.2,