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rs121912737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912737(C;T)
Make rs121912737(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position110340702
GeneATP2A2
is asnp
is mentioned by
dbSNPrs121912737
ebirs121912737
HLIrs121912737
Exacrs121912737
Varsomers121912737
Maprs121912737
PheGenIrs121912737
hapmaprs121912737
1000 genomesrs121912737
hgdprs121912737
ensemblrs121912737
gopubmedrs121912737
geneviewrs121912737
scholarrs121912737
googlers121912737
pharmgkbrs121912737
gwascentralrs121912737
openSNPrs121912737
23andMers121912737
23andMe allrs121912737
SNP Nexus

SNPshotrs121912737
SNPdbers121912737
MSV3drs121912737
GWAS Ctlgrs121912737
Max Magnitude0
OMIM108740
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121912737(T;T)
Alt rs121912737(T;T)
Reference rs121912737(C;C)
Significance Pathogenic
Disease Acrokeratosis verruciformis of Hopf
Variation info
Gene ATP2A2
CLNDBN Acrokeratosis verruciformis of Hopf
Reversed 0
HGVS NC_000012.11:g.110778507C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019377.23,