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rs794727649

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727649(A;G)
Make rs794727649(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position71510080
GeneCDH23, LOC102723377
is asnp
is mentioned by
dbSNPrs794727649
ebirs794727649
HLIrs794727649
Exacrs794727649
Varsomers794727649
Maprs794727649
PheGenIrs794727649
hapmaprs794727649
1000 genomesrs794727649
hgdprs794727649
ensemblrs794727649
gopubmedrs794727649
geneviewrs794727649
scholarrs794727649
googlers794727649
pharmgkbrs794727649
gwascentralrs794727649
openSNPrs794727649
23andMers794727649
23andMe allrs794727649
SNP Nexus

SNPshotrs794727649
SNPdbers794727649
MSV3drs794727649
GWAS Ctlgrs794727649
Max Magnitude0
ClinVar
Risk rs794727649(G;G)
Alt rs794727649(G;G)
Reference rs794727649(A;A)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene LOC102723377 CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73269837A>G
CLNSRC
CLNACC RCV000178332.1,