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rs876657725

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657725(C;T)
Make rs876657725(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position43611237
GeneSTRC
is asnp
is mentioned by
dbSNPrs876657725
ebirs876657725
HLIrs876657725
Exacrs876657725
Varsomers876657725
Maprs876657725
PheGenIrs876657725
hapmaprs876657725
1000 genomesrs876657725
hgdprs876657725
ensemblrs876657725
gopubmedrs876657725
geneviewrs876657725
scholarrs876657725
googlers876657725
pharmgkbrs876657725
gwascentralrs876657725
openSNPrs876657725
23andMers876657725
23andMe allrs876657725
SNP Nexus

SNPshotrs876657725
SNPdbers876657725
MSV3drs876657725
GWAS Ctlgrs876657725
Max Magnitude0
ClinVar
Risk rs876657725(T;T)
Alt rs876657725(T;T)
Reference rs876657725(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.43903435G>A
CLNSRC
CLNACC RCV000218786.1,