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rs727503841

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503841(G;T)
Make rs727503841(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position71734659
GeneCDH23, C10orf105
is asnp
is mentioned by
dbSNPrs727503841
ebirs727503841
HLIrs727503841
Exacrs727503841
Varsomers727503841
Maprs727503841
PheGenIrs727503841
hapmaprs727503841
1000 genomesrs727503841
hgdprs727503841
ensemblrs727503841
gopubmedrs727503841
geneviewrs727503841
scholarrs727503841
googlers727503841
pharmgkbrs727503841
gwascentralrs727503841
openSNPrs727503841
23andMers727503841
23andMe allrs727503841
SNP Nexus

SNPshotrs727503841
SNPdbers727503841
MSV3drs727503841
GWAS Ctlgrs727503841
Max Magnitude0
ClinVar
Risk rs727503841(T;T)
Alt rs727503841(T;T)
Reference rs727503841(G;G)
Significance Pathogenic
Disease not provided Usher syndrome
Variation info
Gene C10orf105 CDH23
CLNDBN not provided Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73494416G>T
CLNSRC
CLNACC RCV000152948.2, RCV000177808.1,