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rs876657653

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657653(C;T)
Make rs876657653(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position75890237
GeneMYO6
is asnp
is mentioned by
dbSNPrs876657653
ebirs876657653
HLIrs876657653
Exacrs876657653
Varsomers876657653
Maprs876657653
PheGenIrs876657653
hapmaprs876657653
1000 genomesrs876657653
hgdprs876657653
ensemblrs876657653
gopubmedrs876657653
geneviewrs876657653
scholarrs876657653
googlers876657653
pharmgkbrs876657653
gwascentralrs876657653
openSNPrs876657653
23andMers876657653
23andMe allrs876657653
SNP Nexus

SNPshotrs876657653
SNPdbers876657653
MSV3drs876657653
GWAS Ctlgrs876657653
Max Magnitude0
ClinVar
Risk rs876657653(T;T)
Alt rs876657653(T;T)
Reference rs876657653(C;C)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO6
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000006.11:g.76599954C>T
CLNSRC
CLNACC RCV000215443.1,