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rs111033415

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033415(A;G)
Make rs111033415(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77162118
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033415
ebirs111033415
HLIrs111033415
Exacrs111033415
Varsomers111033415
Maprs111033415
PheGenIrs111033415
hapmaprs111033415
1000 genomesrs111033415
hgdprs111033415
ensemblrs111033415
gopubmedrs111033415
geneviewrs111033415
scholarrs111033415
googlers111033415
pharmgkbrs111033415
gwascentralrs111033415
openSNPrs111033415
23andMers111033415
23andMe allrs111033415
SNP Nexus

SNPshotrs111033415
SNPdbers111033415
MSV3drs111033415
GWAS Ctlgrs111033415
Max Magnitude0
ClinVar
Risk rs111033415(G;G)
Alt rs111033415(G;G)
Reference rs111033415(A;A)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76873164A>G
CLNSRC ClinVar
CLNACC RCV000036047.2,