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rs397517287

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517287(-;-)
Make rs397517287(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position18154142
GeneMYO15A
is asnp
is mentioned by
dbSNPrs397517287
ebirs397517287
HLIrs397517287
Exacrs397517287
Varsomers397517287
Maprs397517287
PheGenIrs397517287
hapmaprs397517287
1000 genomesrs397517287
hgdprs397517287
ensemblrs397517287
gopubmedrs397517287
geneviewrs397517287
scholarrs397517287
googlers397517287
pharmgkbrs397517287
gwascentralrs397517287
openSNPrs397517287
23andMers397517287
23andMe allrs397517287
SNP Nexus

SNPshotrs397517287
SNPdbers397517287
MSV3drs397517287
GWAS Ctlgrs397517287
Max Magnitude0
ClinVar
Risk rs397517287(;)
Alt rs397517287(;)
Reference rs397517287(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18057456delC
CLNSRC ClinVar
CLNACC RCV000038989.2,