Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909098(A;A)
Make rs121909098(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position57661207
GeneATP8B1, LOC100505549
is asnp
is mentioned by
dbSNPrs121909098
ebirs121909098
HLIrs121909098
Exacrs121909098
Varsomers121909098
Maprs121909098
PheGenIrs121909098
hapmaprs121909098
1000 genomesrs121909098
hgdprs121909098
ensemblrs121909098
gopubmedrs121909098
geneviewrs121909098
scholarrs121909098
googlers121909098
pharmgkbrs121909098
gwascentralrs121909098
openSNPrs121909098
23andMers121909098
23andMe allrs121909098
SNP Nexus

SNPshotrs121909098
SNPdbers121909098
MSV3drs121909098
GWAS Ctlgrs121909098
Max Magnitude0
OMIM602397
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909098(A;A)
Alt rs121909098(A;A)
Reference rs121909098(G;G)
Significance Pathogenic
Disease Progressive intrahepatic cholestasis
Variation info
Gene ATP8B1 LOC100505549
CLNDBN Progressive intrahepatic cholestasis
Reversed 1
HGVS NC_000018.9:g.55328439C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007685.4,