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rs876657680

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657680(G;T)
Make rs876657680(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71646618
GeneCDH23
is asnp
is mentioned by
dbSNPrs876657680
ebirs876657680
HLIrs876657680
Exacrs876657680
Varsomers876657680
Maprs876657680
PheGenIrs876657680
hapmaprs876657680
1000 genomesrs876657680
hgdprs876657680
ensemblrs876657680
gopubmedrs876657680
geneviewrs876657680
scholarrs876657680
googlers876657680
pharmgkbrs876657680
gwascentralrs876657680
openSNPrs876657680
23andMers876657680
23andMe allrs876657680
SNP Nexus

SNPshotrs876657680
SNPdbers876657680
MSV3drs876657680
GWAS Ctlgrs876657680
Max Magnitude0
ClinVar
Risk rs876657680(T;T)
Alt rs876657680(T;T)
Reference rs876657680(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73406375G>T
CLNSRC
CLNACC RCV000215736.1,