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rs773464867

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773464867(C;G)
Make rs773464867(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71812813
GeneCDH23
is asnp
is mentioned by
dbSNPrs773464867
ebirs773464867
HLIrs773464867
Exacrs773464867
Varsomers773464867
Maprs773464867
PheGenIrs773464867
hapmaprs773464867
1000 genomesrs773464867
hgdprs773464867
ensemblrs773464867
gopubmedrs773464867
geneviewrs773464867
scholarrs773464867
googlers773464867
pharmgkbrs773464867
gwascentralrs773464867
openSNPrs773464867
23andMers773464867
23andMe allrs773464867
SNP Nexus

SNPshotrs773464867
SNPdbers773464867
MSV3drs773464867
GWAS Ctlgrs773464867
Max Magnitude0
ClinVar
Risk rs773464867(G;G)
Alt rs773464867(G;G)
Reference rs773464867(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73572570C>T
CLNSRC
CLNACC RCV000214408.1,