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rs779018464

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779018464(C;T)
Make rs779018464(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position20189193
GeneGJB2
is asnp
is mentioned by
dbSNPrs779018464
ebirs779018464
HLIrs779018464
Exacrs779018464
Varsomers779018464
Maprs779018464
PheGenIrs779018464
hapmaprs779018464
1000 genomesrs779018464
hgdprs779018464
ensemblrs779018464
gopubmedrs779018464
geneviewrs779018464
scholarrs779018464
googlers779018464
pharmgkbrs779018464
gwascentralrs779018464
openSNPrs779018464
23andMers779018464
23andMe allrs779018464
SNP Nexus

SNPshotrs779018464
SNPdbers779018464
MSV3drs779018464
GWAS Ctlgrs779018464
Max Magnitude0
ClinVar
Risk rs779018464(T;T)
Alt rs779018464(T;T)
Reference rs779018464(C;C)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene GJB2
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000013.10:g.20763332C>G
CLNSRC
CLNACC RCV000213896.1,