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rs1060499806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499806(G;T)
Make rs1060499806(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position83509169
GenePOU3F4
is asnp
is mentioned by
dbSNPrs1060499806
dbSNP (old)rs1060499806
ClinGenrs1060499806
ebirs1060499806
HLIrs1060499806
Exacrs1060499806
Gnomadrs1060499806
Varsomers1060499806
Maprs1060499806
PheGenIrs1060499806
Biobankrs1060499806
1000 genomesrs1060499806
hgdprs1060499806
ensemblrs1060499806
gopubmedrs1060499806
geneviewrs1060499806
scholarrs1060499806
googlers1060499806
pharmgkbrs1060499806
gwascentralrs1060499806
openSNPrs1060499806
23andMers1060499806
23andMe allrs1060499806
SNPshotrs1060499806
SNPdbers1060499806
MSV3drs1060499806
GWAS Ctlgrs1060499806
Max Magnitude0
ClinVar
Risk rs1060499806(T;T)
Alt rs1060499806(T;T)
Reference Rs1060499806(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene POU3F4
CLNDBN Deafness, X-linked 2
Reversed 0
HGVS NC_000023.10:g.82764177G>T
CLNSRC
CLNACC RCV000454255.1,