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rs1060499799

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499799(G;T)
Make rs1060499799(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position75844977
GeneMYO6
is asnp
is mentioned by
dbSNPrs1060499799
dbSNP (old)rs1060499799
ClinGenrs1060499799
ebirs1060499799
HLIrs1060499799
Exacrs1060499799
Gnomadrs1060499799
Varsomers1060499799
Maprs1060499799
PheGenIrs1060499799
Biobankrs1060499799
1000 genomesrs1060499799
hgdprs1060499799
ensemblrs1060499799
gopubmedrs1060499799
geneviewrs1060499799
scholarrs1060499799
googlers1060499799
pharmgkbrs1060499799
gwascentralrs1060499799
openSNPrs1060499799
23andMers1060499799
23andMe allrs1060499799
SNPshotrs1060499799
SNPdbers1060499799
MSV3drs1060499799
GWAS Ctlgrs1060499799
Max Magnitude0
ClinVar
Risk rs1060499799(T;T)
Alt rs1060499799(T;T)
Reference Rs1060499799(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO6
CLNDBN Deafness, autosomal dominant 22
Reversed 0
HGVS NC_000006.11:g.76554694G>T
CLNSRC
CLNACC RCV000454125.1,