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rs779760634

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779760634(C;T)
Make rs779760634(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position114423524
GeneDFNB31
is asnp
is mentioned by
dbSNPrs779760634
ebirs779760634
HLIrs779760634
Exacrs779760634
Varsomers779760634
Maprs779760634
PheGenIrs779760634
hapmaprs779760634
1000 genomesrs779760634
hgdprs779760634
ensemblrs779760634
gopubmedrs779760634
geneviewrs779760634
scholarrs779760634
googlers779760634
pharmgkbrs779760634
gwascentralrs779760634
openSNPrs779760634
23andMers779760634
23andMe allrs779760634
SNP Nexus

SNPshotrs779760634
SNPdbers779760634
MSV3drs779760634
GWAS Ctlgrs779760634
Max Magnitude0
ClinVar
Risk rs779760634(T;T)
Alt rs779760634(T;T)
Reference rs779760634(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene DFNB31
CLNDBN Deafness, autosomal recessive 31
Reversed 0
HGVS NC_000009.11:g.117185804C>T
CLNSRC
CLNACC RCV000179947.1,