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rs111033486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033486(A;G)
Make rs111033486(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77156900
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033486
ebirs111033486
HLIrs111033486
Exacrs111033486
Varsomers111033486
Maprs111033486
PheGenIrs111033486
hapmaprs111033486
1000 genomesrs111033486
hgdprs111033486
ensemblrs111033486
gopubmedrs111033486
geneviewrs111033486
scholarrs111033486
googlers111033486
pharmgkbrs111033486
gwascentralrs111033486
openSNPrs111033486
23andMers111033486
23andMe allrs111033486
SNP Nexus

SNPshotrs111033486
SNPdbers111033486
MSV3drs111033486
GWAS Ctlgrs111033486
Max Magnitude0
ClinVar
Risk rs111033486(G;G)
Alt rs111033486(G;G)
Reference rs111033486(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76867946A>G
CLNSRC ClinVar
CLNACC RCV000036230.2,