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rs876657724

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657724(A;A)
Make rs876657724(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position43616480
GeneSTRC
is asnp
is mentioned by
dbSNPrs876657724
ebirs876657724
HLIrs876657724
Exacrs876657724
Varsomers876657724
Maprs876657724
PheGenIrs876657724
hapmaprs876657724
1000 genomesrs876657724
hgdprs876657724
ensemblrs876657724
gopubmedrs876657724
geneviewrs876657724
scholarrs876657724
googlers876657724
pharmgkbrs876657724
gwascentralrs876657724
openSNPrs876657724
23andMers876657724
23andMe allrs876657724
SNP Nexus

SNPshotrs876657724
SNPdbers876657724
MSV3drs876657724
GWAS Ctlgrs876657724
Max Magnitude0
ClinVar
Risk rs876657724(A;A)
Alt rs876657724(A;A)
Reference rs876657724(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.43908678G>T
CLNSRC
CLNACC RCV000215137.1,