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rs397517045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517045(-;-)
Make rs397517045(-;G)
Make rs397517045(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position75879853
GeneMYO6
is asnp
is mentioned by
dbSNPrs397517045
ebirs397517045
HLIrs397517045
Exacrs397517045
Varsomers397517045
Maprs397517045
PheGenIrs397517045
hapmaprs397517045
1000 genomesrs397517045
hgdprs397517045
ensemblrs397517045
gopubmedrs397517045
geneviewrs397517045
scholarrs397517045
googlers397517045
pharmgkbrs397517045
gwascentralrs397517045
openSNPrs397517045
23andMers397517045
23andMe allrs397517045
SNP Nexus

SNPshotrs397517045
SNPdbers397517045
MSV3drs397517045
GWAS Ctlgrs397517045
Max Magnitude0
ClinVar
Risk rs397517045(G;G)
Alt rs397517045(G;G)
Reference rs397517045(;)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO6
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000006.11:g.76589570dupG
CLNSRC ClinVar
CLNACC RCV000038290.2,