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rs1060499792

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499792(C;T)
Make rs1060499792(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71677616
GeneCDH23
is asnp
is mentioned by
dbSNPrs1060499792
dbSNP (old)rs1060499792
ClinGenrs1060499792
ebirs1060499792
HLIrs1060499792
Exacrs1060499792
Gnomadrs1060499792
Varsomers1060499792
Maprs1060499792
PheGenIrs1060499792
Biobankrs1060499792
1000 genomesrs1060499792
hgdprs1060499792
ensemblrs1060499792
gopubmedrs1060499792
geneviewrs1060499792
scholarrs1060499792
googlers1060499792
pharmgkbrs1060499792
gwascentralrs1060499792
openSNPrs1060499792
23andMers1060499792
23andMe allrs1060499792
SNPshotrs1060499792
SNPdbers1060499792
MSV3drs1060499792
GWAS Ctlgrs1060499792
Max Magnitude0
ClinVar
Risk rs1060499792(T;T)
Alt rs1060499792(T;T)
Reference Rs1060499792(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73437373C>T
CLNSRC
CLNACC RCV000454185.1,