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rs111033284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033284(A;A)
Make rs111033284(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77156991
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033284
ebirs111033284
HLIrs111033284
Exacrs111033284
Varsomers111033284
Maprs111033284
PheGenIrs111033284
hapmaprs111033284
1000 genomesrs111033284
hgdprs111033284
ensemblrs111033284
gopubmedrs111033284
geneviewrs111033284
scholarrs111033284
googlers111033284
pharmgkbrs111033284
gwascentralrs111033284
openSNPrs111033284
23andMers111033284
23andMe allrs111033284
SNP Nexus

SNPshotrs111033284
SNPdbers111033284
MSV3drs111033284
GWAS Ctlgrs111033284
Max Magnitude0
ClinVar
Risk rs111033284(A;A)
Alt rs111033284(A;A)
Reference rs111033284(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76868037G>A
CLNSRC ClinVar
CLNACC RCV000036247.2,