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rs1060499793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499793(A;A)
Make rs1060499793(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71709172
GeneCDH23
is asnp
is mentioned by
dbSNPrs1060499793
dbSNP (old)rs1060499793
ClinGenrs1060499793
ebirs1060499793
HLIrs1060499793
Exacrs1060499793
Gnomadrs1060499793
Varsomers1060499793
LitVarrs1060499793
Maprs1060499793
PheGenIrs1060499793
Biobankrs1060499793
1000 genomesrs1060499793
hgdprs1060499793
ensemblrs1060499793
gopubmedrs1060499793
geneviewrs1060499793
scholarrs1060499793
googlers1060499793
pharmgkbrs1060499793
gwascentralrs1060499793
openSNPrs1060499793
23andMers1060499793
23andMe allrs1060499793
SNPshotrs1060499793
SNPdbers1060499793
MSV3drs1060499793
GWAS Ctlgrs1060499793
Max Magnitude0
ClinVar
Risk rs1060499793(A;A)
Alt rs1060499793(A;A)
Reference Rs1060499793(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73468929G>A
CLNSRC
CLNACC RCV000454274.1,