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rs1060499790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499790(C;C)
Make rs1060499790(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71807302
GeneCDH23
is asnp
is mentioned by
dbSNPrs1060499790
dbSNP (classic)rs1060499790
ClinGenrs1060499790
ebirs1060499790
HLIrs1060499790
Exacrs1060499790
Gnomadrs1060499790
Varsomers1060499790
LitVarrs1060499790
Maprs1060499790
PheGenIrs1060499790
Biobankrs1060499790
1000 genomesrs1060499790
hgdprs1060499790
ensemblrs1060499790
geneviewrs1060499790
scholarrs1060499790
googlers1060499790
pharmgkbrs1060499790
gwascentralrs1060499790
openSNPrs1060499790
23andMers1060499790
23andMe allrs1060499790
SNPshotrs1060499790
SNPdbers1060499790
MSV3drs1060499790
GWAS Ctlgrs1060499790
Max Magnitude0
ClinVar
Risk rs1060499790(C;C)
Alt rs1060499790(C;C)
Reference Rs1060499790(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73567059T>C
CLNSRC
CLNACC RCV000454163.1,