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rs181611778

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs181611778(A;A)
Make rs181611778(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71778252
GeneCDH23
is asnp
is mentioned by
dbSNPrs181611778
dbSNP (classic)rs181611778
ClinGenrs181611778
ebirs181611778
HLIrs181611778
Exacrs181611778
Gnomadrs181611778
Varsomers181611778
LitVarrs181611778
Maprs181611778
PheGenIrs181611778
Biobankrs181611778
1000 genomesrs181611778
hgdprs181611778
ensemblrs181611778
geneviewrs181611778
scholarrs181611778
googlers181611778
pharmgkbrs181611778
gwascentralrs181611778
openSNPrs181611778
23andMers181611778
23andMe allrs181611778
SNPshotrs181611778
SNPdbers181611778
MSV3drs181611778
GWAS Ctlgrs181611778
Max Magnitude0
ClinVar
Risk rs181611778(A;A)
Alt rs181611778(A;A)
Reference Rs181611778(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene CDH23
CLNDBN not specified not provided
Reversed 0
HGVS NC_000010.10:g.73538009G>A
CLNSRC
CLNACC RCV000178447.1, RCV000479783.1,