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rs1060499789

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499789(A;A)
Make rs1060499789(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71785667
GeneCDH23
is asnp
is mentioned by
dbSNPrs1060499789
dbSNP (old)rs1060499789
ClinGenrs1060499789
ebirs1060499789
HLIrs1060499789
Exacrs1060499789
Gnomadrs1060499789
Varsomers1060499789
Maprs1060499789
PheGenIrs1060499789
Biobankrs1060499789
1000 genomesrs1060499789
hgdprs1060499789
ensemblrs1060499789
gopubmedrs1060499789
geneviewrs1060499789
scholarrs1060499789
googlers1060499789
pharmgkbrs1060499789
gwascentralrs1060499789
openSNPrs1060499789
23andMers1060499789
23andMe allrs1060499789
SNPshotrs1060499789
SNPdbers1060499789
MSV3drs1060499789
GWAS Ctlgrs1060499789
Max Magnitude0
ClinVar
Risk rs1060499789(A;A)
Alt rs1060499789(A;A)
Reference Rs1060499789(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73545424G>A
CLNSRC
CLNACC RCV000454137.1,