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rs121909101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909101(A;A)
Make rs121909101(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position57674993
GeneATP8B1
is asnp
is mentioned by
dbSNPrs121909101
ebirs121909101
HLIrs121909101
Exacrs121909101
Varsomers121909101
Maprs121909101
PheGenIrs121909101
hapmaprs121909101
1000 genomesrs121909101
hgdprs121909101
ensemblrs121909101
gopubmedrs121909101
geneviewrs121909101
scholarrs121909101
googlers121909101
pharmgkbrs121909101
gwascentralrs121909101
openSNPrs121909101
23andMers121909101
23andMe allrs121909101
SNP Nexus

SNPshotrs121909101
SNPdbers121909101
MSV3drs121909101
GWAS Ctlgrs121909101
Max Magnitude0
OMIM602397
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121909101(A;A)
Alt rs121909101(A;A)
Reference rs121909101(G;G)
Significance Pathogenic
Disease Progressive intrahepatic cholestasis
Variation info
Gene ATP8B1
CLNDBN Progressive intrahepatic cholestasis
Reversed 1
HGVS NC_000018.9:g.55342225C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007692.4,