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rs876657726

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657726(C;T)
Make rs876657726(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position43610317
GeneSTRC
is asnp
is mentioned by
dbSNPrs876657726
ebirs876657726
HLIrs876657726
Exacrs876657726
Varsomers876657726
Maprs876657726
PheGenIrs876657726
hapmaprs876657726
1000 genomesrs876657726
hgdprs876657726
ensemblrs876657726
gopubmedrs876657726
geneviewrs876657726
scholarrs876657726
googlers876657726
pharmgkbrs876657726
gwascentralrs876657726
openSNPrs876657726
23andMers876657726
23andMe allrs876657726
SNP Nexus

SNPshotrs876657726
SNPdbers876657726
MSV3drs876657726
GWAS Ctlgrs876657726
Max Magnitude0
ClinVar
Risk rs876657726(T;T)
Alt rs876657726(T;T)
Reference rs876657726(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene STRC
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000015.9:g.43902515G>A
CLNSRC
CLNACC RCV000222381.1,