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rs1060499788

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499788(A;T)
Make rs1060499788(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71570848
GeneCDH23
is asnp
is mentioned by
dbSNPrs1060499788
dbSNP (old)rs1060499788
ClinGenrs1060499788
ebirs1060499788
HLIrs1060499788
Exacrs1060499788
Gnomadrs1060499788
Varsomers1060499788
LitVarrs1060499788
Maprs1060499788
PheGenIrs1060499788
Biobankrs1060499788
1000 genomesrs1060499788
hgdprs1060499788
ensemblrs1060499788
gopubmedrs1060499788
geneviewrs1060499788
scholarrs1060499788
googlers1060499788
pharmgkbrs1060499788
gwascentralrs1060499788
openSNPrs1060499788
23andMers1060499788
23andMe allrs1060499788
SNPshotrs1060499788
SNPdbers1060499788
MSV3drs1060499788
GWAS Ctlgrs1060499788
Max Magnitude0
ClinVar
Risk rs1060499788(T;T)
Alt rs1060499788(T;T)
Reference Rs1060499788(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene LOC101929085 CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73330605A>T
CLNSRC
CLNACC RCV000454219.1,