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rs1057519500

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519500(A;A)
Make rs1057519500(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71566790
GeneCDH23
is asnp
is mentioned by
dbSNPrs1057519500
dbSNP (old)rs1057519500
ClinGenrs1057519500
ebirs1057519500
HLIrs1057519500
Exacrs1057519500
Gnomadrs1057519500
Varsomers1057519500
LitVarrs1057519500
Maprs1057519500
PheGenIrs1057519500
Biobankrs1057519500
1000 genomesrs1057519500
hgdprs1057519500
ensemblrs1057519500
gopubmedrs1057519500
geneviewrs1057519500
scholarrs1057519500
googlers1057519500
pharmgkbrs1057519500
gwascentralrs1057519500
openSNPrs1057519500
23andMers1057519500
23andMe allrs1057519500
SNPshotrs1057519500
SNPdbers1057519500
MSV3drs1057519500
GWAS Ctlgrs1057519500
Max Magnitude0
ClinVar
Risk rs1057519500(A;A)
Alt rs1057519500(A;A)
Reference Rs1057519500(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene LOC101929085 CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73326547G>A
CLNSRC
CLNACC RCV000416554.1,