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rs121434451

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434451(A;A)
Make rs121434451(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position22119227
GeneHR
is asnp
is mentioned by
dbSNPrs121434451
ebirs121434451
HLIrs121434451
Exacrs121434451
Varsomers121434451
Maprs121434451
PheGenIrs121434451
hapmaprs121434451
1000 genomesrs121434451
hgdprs121434451
ensemblrs121434451
gopubmedrs121434451
geneviewrs121434451
scholarrs121434451
googlers121434451
pharmgkbrs121434451
gwascentralrs121434451
openSNPrs121434451
23andMers121434451
23andMe allrs121434451
SNP Nexus

SNPshotrs121434451
SNPdbers121434451
MSV3drs121434451
GWAS Ctlgrs121434451
Max Magnitude0
OMIM602302
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121434451(A;A)
Alt rs121434451(A;A)
Reference rs121434451(G;G)
Significance Pathogenic
Disease Alopecia universalis congenita
Variation info
Gene HR
CLNDBN Alopecia universalis congenita
Reversed 1
HGVS NC_000008.10:g.21976740C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007765.3,