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rs387906382

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906382(C;C)
Make rs387906382(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position22130707
GeneHR
is asnp
is mentioned by
dbSNPrs387906382
ebirs387906382
HLIrs387906382
Exacrs387906382
Varsomers387906382
Maprs387906382
PheGenIrs387906382
hapmaprs387906382
1000 genomesrs387906382
hgdprs387906382
ensemblrs387906382
gopubmedrs387906382
geneviewrs387906382
scholarrs387906382
googlers387906382
pharmgkbrs387906382
gwascentralrs387906382
openSNPrs387906382
23andMers387906382
23andMe allrs387906382
SNP Nexus

SNPshotrs387906382
SNPdbers387906382
MSV3drs387906382
GWAS Ctlgrs387906382
Max Magnitude0
ClinVar
Risk rs387906382(C;C)
Alt rs387906382(C;C)
Reference rs387906382(T;T)
Significance Pathogenic
Disease Hypotrichosis 4
Variation info
Gene HR
CLNDBN Hypotrichosis 4
Reversed 1
HGVS NC_000008.10:g.21988220A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007766.3,