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rs1060499791

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499791(C;T)
Make rs1060499791(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71617295
GeneCDH23
is asnp
is mentioned by
dbSNPrs1060499791
dbSNP (old)rs1060499791
ClinGenrs1060499791
ebirs1060499791
HLIrs1060499791
Exacrs1060499791
Gnomadrs1060499791
Varsomers1060499791
Maprs1060499791
PheGenIrs1060499791
Biobankrs1060499791
1000 genomesrs1060499791
hgdprs1060499791
ensemblrs1060499791
gopubmedrs1060499791
geneviewrs1060499791
scholarrs1060499791
googlers1060499791
pharmgkbrs1060499791
gwascentralrs1060499791
openSNPrs1060499791
23andMers1060499791
23andMe allrs1060499791
SNPshotrs1060499791
SNPdbers1060499791
MSV3drs1060499791
GWAS Ctlgrs1060499791
Max Magnitude0
ClinVar
Risk rs1060499791(T;T)
Alt rs1060499791(T;T)
Reference Rs1060499791(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73377052C>T
CLNSRC
CLNACC RCV000454253.1,