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rs111033182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033182(C;T)
Make rs111033182(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77202357
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033182
ebirs111033182
HLIrs111033182
Exacrs111033182
Varsomers111033182
Maprs111033182
PheGenIrs111033182
hapmaprs111033182
1000 genomesrs111033182
hgdprs111033182
ensemblrs111033182
gopubmedrs111033182
geneviewrs111033182
scholarrs111033182
googlers111033182
pharmgkbrs111033182
gwascentralrs111033182
openSNPrs111033182
23andMers111033182
23andMe allrs111033182
SNP Nexus

SNPshotrs111033182
SNPdbers111033182
MSV3drs111033182
GWAS Ctlgrs111033182
Max Magnitude0
ClinVar
Risk rs111033182(T;T)
Alt rs111033182(T;T)
Reference rs111033182(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76913402C>T
CLNSRC ClinVar
CLNACC RCV000036175.2,