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rs876657682

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657682(C;C)
Make rs876657682(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71802897
GeneCDH23
is asnp
is mentioned by
dbSNPrs876657682
ebirs876657682
HLIrs876657682
Exacrs876657682
Varsomers876657682
Maprs876657682
PheGenIrs876657682
hapmaprs876657682
1000 genomesrs876657682
hgdprs876657682
ensemblrs876657682
gopubmedrs876657682
geneviewrs876657682
scholarrs876657682
googlers876657682
pharmgkbrs876657682
gwascentralrs876657682
openSNPrs876657682
23andMers876657682
23andMe allrs876657682
SNP Nexus

SNPshotrs876657682
SNPdbers876657682
MSV3drs876657682
GWAS Ctlgrs876657682
Max Magnitude0
ClinVar
Risk rs876657682(C;C)
Alt rs876657682(C;C)
Reference rs876657682(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73562654G>C
CLNSRC
CLNACC RCV000221407.1,