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rs876657710

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657710(C;G)
Make rs876657710(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position75832908
GeneMYO6
is asnp
is mentioned by
dbSNPrs876657710
ebirs876657710
HLIrs876657710
Exacrs876657710
Varsomers876657710
Maprs876657710
PheGenIrs876657710
hapmaprs876657710
1000 genomesrs876657710
hgdprs876657710
ensemblrs876657710
gopubmedrs876657710
geneviewrs876657710
scholarrs876657710
googlers876657710
pharmgkbrs876657710
gwascentralrs876657710
openSNPrs876657710
23andMers876657710
23andMe allrs876657710
SNP Nexus

SNPshotrs876657710
SNPdbers876657710
MSV3drs876657710
GWAS Ctlgrs876657710
Max Magnitude0
ClinVar
Risk rs876657710(G;G)
Alt rs876657710(G;G)
Reference rs876657710(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO6
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000006.11:g.76542625C>G
CLNSRC
CLNACC RCV000216690.1,