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rs515726138

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726138(G;T)
Make rs515726138(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position57697797
GeneATP8B1
is asnp
is mentioned by
dbSNPrs515726138
ebirs515726138
HLIrs515726138
Exacrs515726138
Varsomers515726138
Maprs515726138
PheGenIrs515726138
hapmaprs515726138
1000 genomesrs515726138
hgdprs515726138
ensemblrs515726138
gopubmedrs515726138
geneviewrs515726138
scholarrs515726138
googlers515726138
pharmgkbrs515726138
gwascentralrs515726138
openSNPrs515726138
23andMers515726138
23andMe allrs515726138
SNP Nexus

SNPshotrs515726138
SNPdbers515726138
MSV3drs515726138
GWAS Ctlgrs515726138
Max Magnitude0
ClinVar
Risk rs515726138(T;T)
Alt rs515726138(T;T)
Reference rs515726138(G;G)
Significance Pathogenic
Disease Progressive intrahepatic cholestasis
Variation info
Gene ATP8B1
CLNDBN Progressive intrahepatic cholestasis
Reversed 0
HGVS NC_000018.9:g.55365029G>T
CLNSRC ClinVar
CLNACC RCV000114322.2,