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rs367928692

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367928692(A;A)
Make rs367928692(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71791123
GeneCDH23
is asnp
is mentioned by
dbSNPrs367928692
ebirs367928692
HLIrs367928692
Exacrs367928692
Varsomers367928692
Maprs367928692
PheGenIrs367928692
hapmaprs367928692
1000 genomesrs367928692
hgdprs367928692
ensemblrs367928692
gopubmedrs367928692
geneviewrs367928692
scholarrs367928692
googlers367928692
pharmgkbrs367928692
gwascentralrs367928692
openSNPrs367928692
23andMers367928692
23andMe allrs367928692
SNP Nexus

SNPshotrs367928692
SNPdbers367928692
MSV3drs367928692
GWAS Ctlgrs367928692
Max Magnitude0
ClinVar
Risk rs367928692(A;A)
Alt rs367928692(A;A)
Reference rs367928692(G;G)
Significance Pathogenic
Disease Usher syndrome not provided
Variation info
Gene MIR7152 CDH23
CLNDBN Usher syndrome, type 1D not provided
Reversed 0
HGVS NC_000010.10:g.73550880G>A
CLNSRC ClinVar
CLNACC RCV000039236.3, RCV000239237.1,