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rs121912422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912422(A;T)
Make rs121912422(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position154588582
GeneADAR
is asnp
is mentioned by
dbSNPrs121912422
ebirs121912422
HLIrs121912422
Exacrs121912422
Varsomers121912422
Maprs121912422
PheGenIrs121912422
hapmaprs121912422
1000 genomesrs121912422
hgdprs121912422
ensemblrs121912422
gopubmedrs121912422
geneviewrs121912422
scholarrs121912422
googlers121912422
pharmgkbrs121912422
gwascentralrs121912422
openSNPrs121912422
23andMers121912422
23andMe allrs121912422
SNP Nexus

SNPshotrs121912422
SNPdbers121912422
MSV3drs121912422
GWAS Ctlgrs121912422
Max Magnitude0
OMIM146920
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912422(T;T)
Alt rs121912422(T;T)
Reference rs121912422(A;A)
Significance Pathogenic
Disease Symmetrical dyschromatosis of extremities
Variation info
Gene ADAR
CLNDBN Symmetrical dyschromatosis of extremities
Reversed 1
HGVS NC_000001.10:g.154561058T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015942.25,