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rs397517285

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517285(A;A)
Make rs397517285(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position18148784
GeneLOC105371568, MYO15A
is asnp
is mentioned by
dbSNPrs397517285
ebirs397517285
HLIrs397517285
Exacrs397517285
Varsomers397517285
Maprs397517285
PheGenIrs397517285
hapmaprs397517285
1000 genomesrs397517285
hgdprs397517285
ensemblrs397517285
gopubmedrs397517285
geneviewrs397517285
scholarrs397517285
googlers397517285
pharmgkbrs397517285
gwascentralrs397517285
openSNPrs397517285
23andMers397517285
23andMe allrs397517285
SNP Nexus

SNPshotrs397517285
SNPdbers397517285
MSV3drs397517285
GWAS Ctlgrs397517285
Max Magnitude0
ClinVar
Risk rs397517285(A;A)
Alt rs397517285(A;A)
Reference rs397517285(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18052098G>A
CLNSRC
CLNACC RCV000038980.2,