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rs397517286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517286(-;-)
Make rs397517286(-;C)
Make rs397517286(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position18149265
GeneMYO15A
is asnp
is mentioned by
dbSNPrs397517286
ebirs397517286
HLIrs397517286
Exacrs397517286
Varsomers397517286
Maprs397517286
PheGenIrs397517286
hapmaprs397517286
1000 genomesrs397517286
hgdprs397517286
ensemblrs397517286
gopubmedrs397517286
geneviewrs397517286
scholarrs397517286
googlers397517286
pharmgkbrs397517286
gwascentralrs397517286
openSNPrs397517286
23andMers397517286
23andMe allrs397517286
SNP Nexus

SNPshotrs397517286
SNPdbers397517286
MSV3drs397517286
GWAS Ctlgrs397517286
Max Magnitude0
ClinVar
Risk rs397517286(C;C)
Alt rs397517286(C;C)
Reference rs397517286(;)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18052579dupC
CLNSRC ClinVar
CLNACC RCV000038981.2,