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rs876661402

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661402(C;T)
Make rs876661402(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position109368871
GeneCD164
is asnp
is mentioned by
dbSNPrs876661402
ebirs876661402
HLIrs876661402
Exacrs876661402
Varsomers876661402
Maprs876661402
PheGenIrs876661402
hapmaprs876661402
1000 genomesrs876661402
hgdprs876661402
ensemblrs876661402
gopubmedrs876661402
geneviewrs876661402
scholarrs876661402
googlers876661402
pharmgkbrs876661402
gwascentralrs876661402
openSNPrs876661402
23andMers876661402
23andMe allrs876661402
SNP Nexus

SNPshotrs876661402
SNPdbers876661402
MSV3drs876661402
GWAS Ctlgrs876661402
Max Magnitude0
ClinVar
Risk rs876661402(T;T)
Alt rs876661402(T;T)
Reference rs876661402(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene CD164
CLNDBN Deafness, autosomal dominant 66
Reversed 1
HGVS NC_000006.11:g.109690074G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000223938.1,