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rs1060499804

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499804(A;T)
Make rs1060499804(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position21705213
GeneOTOA
is asnp
is mentioned by
dbSNPrs1060499804
dbSNP (old)rs1060499804
ClinGenrs1060499804
ebirs1060499804
HLIrs1060499804
Exacrs1060499804
Gnomadrs1060499804
Varsomers1060499804
Maprs1060499804
PheGenIrs1060499804
Biobankrs1060499804
1000 genomesrs1060499804
hgdprs1060499804
ensemblrs1060499804
gopubmedrs1060499804
geneviewrs1060499804
scholarrs1060499804
googlers1060499804
pharmgkbrs1060499804
gwascentralrs1060499804
openSNPrs1060499804
23andMers1060499804
23andMe allrs1060499804
SNPshotrs1060499804
SNPdbers1060499804
MSV3drs1060499804
GWAS Ctlgrs1060499804
Max Magnitude0
ClinVar
Risk rs1060499804(T;T)
Alt rs1060499804(T;T)
Reference Rs1060499804(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOA
CLNDBN Deafness, autosomal recessive 22
Reversed 0
HGVS NC_000016.9:g.21716534A>T
CLNSRC
CLNACC RCV000454173.1,