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rs1060499651

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs1060499651(-;-)
Make rs1060499651(-;GT)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77156754
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1060499651
dbSNP (old)rs1060499651
ClinGenrs1060499651
ebirs1060499651
HLIrs1060499651
Exacrs1060499651
Gnomadrs1060499651
Varsomers1060499651
Maprs1060499651
PheGenIrs1060499651
Biobankrs1060499651
1000 genomesrs1060499651
hgdprs1060499651
ensemblrs1060499651
gopubmedrs1060499651
geneviewrs1060499651
scholarrs1060499651
googlers1060499651
pharmgkbrs1060499651
gwascentralrs1060499651
openSNPrs1060499651
23andMers1060499651
23andMe allrs1060499651
SNPshotrs1060499651
SNPdbers1060499651
MSV3drs1060499651
GWAS Ctlgrs1060499651
Max Magnitude0
ClinVar
Risk rs1060499651(-;-)
Alt rs1060499651(-;-)
Reference Rs1060499651(GT;GT)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76867800_76867801delGT
CLNSRC
CLNACC RCV000449499.1,