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rs767178508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 3 Carrier of a recessive deafness mutation
(C;C) 0 common/normal
(C;T) 3 Carrier of a recessive deafness mutation


Make rs767178508(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position20189143
GeneGJB2
is asnp
is mentioned by
dbSNPrs767178508
ebirs767178508
HLIrs767178508
Exacrs767178508
Varsomers767178508
Maprs767178508
PheGenIrs767178508
hapmaprs767178508
1000 genomesrs767178508
hgdprs767178508
ensemblrs767178508
gopubmedrs767178508
geneviewrs767178508
scholarrs767178508
googlers767178508
pharmgkbrs767178508
gwascentralrs767178508
openSNPrs767178508
23andMers767178508
23andMe allrs767178508
SNP Nexus

SNPshotrs767178508
SNPdbers767178508
MSV3drs767178508
GWAS Ctlgrs767178508
Max Magnitude3
note both c.439G>T and c.439G>A GJB2 mutations are considered pathogenic for deafness