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rs727502919

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727502919(G;T)
Make rs727502919(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position71615617
GeneCDH23
is asnp
is mentioned by
dbSNPrs727502919
ebirs727502919
HLIrs727502919
Exacrs727502919
Varsomers727502919
Maprs727502919
PheGenIrs727502919
hapmaprs727502919
1000 genomesrs727502919
hgdprs727502919
ensemblrs727502919
gopubmedrs727502919
geneviewrs727502919
scholarrs727502919
googlers727502919
pharmgkbrs727502919
gwascentralrs727502919
openSNPrs727502919
23andMers727502919
23andMe allrs727502919
SNP Nexus

SNPshotrs727502919
SNPdbers727502919
MSV3drs727502919
GWAS Ctlgrs727502919
Max Magnitude0
ClinVar
Risk rs727502919(T;T)
Alt rs727502919(T;T)
Reference rs727502919(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73375374G>T
CLNSRC
CLNACC RCV000150272.1,