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rs876657681

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657681(-;-)
Make rs876657681(-;C)
Make rs876657681(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71682535
GeneCDH23
is asnp
is mentioned by
dbSNPrs876657681
ebirs876657681
HLIrs876657681
Exacrs876657681
Varsomers876657681
Maprs876657681
PheGenIrs876657681
hapmaprs876657681
1000 genomesrs876657681
hgdprs876657681
ensemblrs876657681
gopubmedrs876657681
geneviewrs876657681
scholarrs876657681
googlers876657681
pharmgkbrs876657681
gwascentralrs876657681
openSNPrs876657681
23andMers876657681
23andMe allrs876657681
SNP Nexus

SNPshotrs876657681
SNPdbers876657681
MSV3drs876657681
GWAS Ctlgrs876657681
Max Magnitude0
ClinVar
Risk rs876657681(C;C)
Alt rs876657681(C;C)
Reference rs876657681(;)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73442292dupC
CLNSRC
CLNACC RCV000218031.1,