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rs876657652

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657652(C;C)
Make rs876657652(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position26193312
GeneLOC105376458, MYO3A
is asnp
is mentioned by
dbSNPrs876657652
ebirs876657652
HLIrs876657652
Exacrs876657652
Varsomers876657652
Maprs876657652
PheGenIrs876657652
hapmaprs876657652
1000 genomesrs876657652
hgdprs876657652
ensemblrs876657652
gopubmedrs876657652
geneviewrs876657652
scholarrs876657652
googlers876657652
pharmgkbrs876657652
gwascentralrs876657652
openSNPrs876657652
23andMers876657652
23andMe allrs876657652
SNP Nexus

SNPshotrs876657652
SNPdbers876657652
MSV3drs876657652
GWAS Ctlgrs876657652
Max Magnitude0
ClinVar
Risk rs876657652(C;C)
Alt rs876657652(C;C)
Reference rs876657652(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO3A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000010.10:g.26482241G>C
CLNSRC
CLNACC RCV000221092.1,