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rs1060499798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499798(A;A)
Make rs1060499798(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18132486
GeneMYO15A
is asnp
is mentioned by
dbSNPrs1060499798
dbSNP (old)rs1060499798
ClinGenrs1060499798
ebirs1060499798
HLIrs1060499798
Exacrs1060499798
Gnomadrs1060499798
Varsomers1060499798
Maprs1060499798
PheGenIrs1060499798
Biobankrs1060499798
1000 genomesrs1060499798
hgdprs1060499798
ensemblrs1060499798
gopubmedrs1060499798
geneviewrs1060499798
scholarrs1060499798
googlers1060499798
pharmgkbrs1060499798
gwascentralrs1060499798
openSNPrs1060499798
23andMers1060499798
23andMe allrs1060499798
SNPshotrs1060499798
SNPdbers1060499798
MSV3drs1060499798
GWAS Ctlgrs1060499798
Max Magnitude0
ClinVar
Risk rs1060499798(A;A)
Alt rs1060499798(A;A)
Reference Rs1060499798(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18035800G>A
CLNSRC
CLNACC RCV000454215.1,