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rs111033175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033175(A;G)
Make rs111033175(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77208781
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033175
ebirs111033175
HLIrs111033175
Exacrs111033175
Varsomers111033175
Maprs111033175
PheGenIrs111033175
hapmaprs111033175
1000 genomesrs111033175
hgdprs111033175
ensemblrs111033175
gopubmedrs111033175
geneviewrs111033175
scholarrs111033175
googlers111033175
pharmgkbrs111033175
gwascentralrs111033175
openSNPrs111033175
23andMers111033175
23andMe allrs111033175
SNP Nexus

SNPshotrs111033175
SNPdbers111033175
MSV3drs111033175
GWAS Ctlgrs111033175
Max Magnitude0
ClinVar
Risk rs111033175(G;G)
Alt rs111033175(G;G)
Reference rs111033175(A;A)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76919826A>G
CLNSRC ClinVar
CLNACC RCV000036219.2,