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

rs121912735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912735(A;A)
Make rs121912735(A;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position110345323
GeneATP2A2
is asnp
is mentioned by
dbSNPrs121912735
ebirs121912735
HLIrs121912735
Exacrs121912735
Varsomers121912735
Maprs121912735
PheGenIrs121912735
hapmaprs121912735
1000 genomesrs121912735
hgdprs121912735
ensemblrs121912735
gopubmedrs121912735
geneviewrs121912735
scholarrs121912735
googlers121912735
pharmgkbrs121912735
gwascentralrs121912735
openSNPrs121912735
23andMers121912735
23andMe allrs121912735
SNP Nexus

SNPshotrs121912735
SNPdbers121912735
MSV3drs121912735
GWAS Ctlgrs121912735
Max Magnitude0
OMIM108740
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121912735(A,T;A,T)
Alt rs121912735(A,T;A,T)
Reference rs121912735(C;C)
Significance Pathogenic
Disease Darier disease
Variation info
Gene ATP2A2
CLNDBN Darier disease, segmental
Reversed 0
HGVS NC_000012.11:g.110783128C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019375.27,