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rs369396703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369396703(A;A)
Make rs369396703(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71677444
GeneCDH23
is asnp
is mentioned by
dbSNPrs369396703
dbSNP (classic)rs369396703
ClinGenrs369396703
ebirs369396703
HLIrs369396703
Exacrs369396703
Gnomadrs369396703
Varsomers369396703
LitVarrs369396703
Maprs369396703
PheGenIrs369396703
Biobankrs369396703
1000 genomesrs369396703
hgdprs369396703
ensemblrs369396703
geneviewrs369396703
scholarrs369396703
googlers369396703
pharmgkbrs369396703
gwascentralrs369396703
openSNPrs369396703
23andMers369396703
23andMe allrs369396703
SNPshotrs369396703
SNPdbers369396703
MSV3drs369396703
GWAS Ctlgrs369396703
Max Magnitude0
ClinVar
Risk rs369396703(A;A)
Alt rs369396703(A;A)
Reference Rs369396703(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.73437201G>A
CLNSRC
CLNACC RCV000216452.1, RCV000486086.1,