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rs876657709

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs876657709(-;-)
Make rs876657709(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position75890212
GeneMYO6
is asnp
is mentioned by
dbSNPrs876657709
ebirs876657709
HLIrs876657709
Exacrs876657709
Varsomers876657709
Maprs876657709
PheGenIrs876657709
hapmaprs876657709
1000 genomesrs876657709
hgdprs876657709
ensemblrs876657709
gopubmedrs876657709
geneviewrs876657709
scholarrs876657709
googlers876657709
pharmgkbrs876657709
gwascentralrs876657709
openSNPrs876657709
23andMers876657709
23andMe allrs876657709
SNP Nexus

SNPshotrs876657709
SNPdbers876657709
MSV3drs876657709
GWAS Ctlgrs876657709
Max Magnitude0
ClinVar
Risk rs876657709(;)
Alt rs876657709(;)
Reference rs876657709(AA;AA)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO6
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000006.11:g.76599929_76599930delAA
CLNSRC
CLNACC RCV000223613.1,