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rs369501114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369501114(A;A)
Make rs369501114(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71806186
GeneCDH23
is asnp
is mentioned by
dbSNPrs369501114
dbSNP (classic)rs369501114
ClinGenrs369501114
ebirs369501114
HLIrs369501114
Exacrs369501114
Gnomadrs369501114
Varsomers369501114
LitVarrs369501114
Maprs369501114
PheGenIrs369501114
Biobankrs369501114
1000 genomesrs369501114
hgdprs369501114
ensemblrs369501114
geneviewrs369501114
scholarrs369501114
googlers369501114
pharmgkbrs369501114
gwascentralrs369501114
openSNPrs369501114
23andMers369501114
23andMe allrs369501114
SNPshotrs369501114
SNPdbers369501114
MSV3drs369501114
GWAS Ctlgrs369501114
Max Magnitude0
ClinVar
Risk rs369501114(A;A)
Alt rs369501114(A;A)
Reference Rs369501114(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDH23
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.73565943G>A
CLNSRC
CLNACC RCV000485626.1,