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rs876657636

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657636(A;A)
Make rs876657636(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71702662
GeneCDH23
is asnp
is mentioned by
dbSNPrs876657636
ebirs876657636
HLIrs876657636
Exacrs876657636
Varsomers876657636
Maprs876657636
PheGenIrs876657636
hapmaprs876657636
1000 genomesrs876657636
hgdprs876657636
ensemblrs876657636
gopubmedrs876657636
geneviewrs876657636
scholarrs876657636
googlers876657636
pharmgkbrs876657636
gwascentralrs876657636
openSNPrs876657636
23andMers876657636
23andMe allrs876657636
SNP Nexus

SNPshotrs876657636
SNPdbers876657636
MSV3drs876657636
GWAS Ctlgrs876657636
Max Magnitude0
ClinVar
Risk rs876657636(A;A)
Alt rs876657636(A;A)
Reference rs876657636(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73462419G>A
CLNSRC
CLNACC RCV000220607.1,