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rs267606867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606867(C;T)
Make rs267606867(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position22130702
GeneHR
is asnp
is mentioned by
dbSNPrs267606867
ebirs267606867
HLIrs267606867
Exacrs267606867
Varsomers267606867
Maprs267606867
PheGenIrs267606867
hapmaprs267606867
1000 genomesrs267606867
hgdprs267606867
ensemblrs267606867
gopubmedrs267606867
geneviewrs267606867
scholarrs267606867
googlers267606867
pharmgkbrs267606867
gwascentralrs267606867
openSNPrs267606867
23andMers267606867
23andMe allrs267606867
SNP Nexus

SNPshotrs267606867
SNPdbers267606867
MSV3drs267606867
GWAS Ctlgrs267606867
Max Magnitude0
ClinVar
Risk rs267606867(T;T)
Alt rs267606867(T;T)
Reference rs267606867(C;C)
Significance Pathogenic
Disease Hypotrichosis 4
Variation info
Gene HR
CLNDBN Hypotrichosis 4
Reversed 1
HGVS NC_000008.10:g.21988215G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007767.3,