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rs111033433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033433(-;-)
Make rs111033433(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77183109
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033433
ebirs111033433
HLIrs111033433
Exacrs111033433
Varsomers111033433
Maprs111033433
PheGenIrs111033433
hapmaprs111033433
1000 genomesrs111033433
hgdprs111033433
ensemblrs111033433
gopubmedrs111033433
geneviewrs111033433
scholarrs111033433
googlers111033433
pharmgkbrs111033433
gwascentralrs111033433
openSNPrs111033433
23andMers111033433
23andMe allrs111033433
SNP Nexus

SNPshotrs111033433
SNPdbers111033433
MSV3drs111033433
GWAS Ctlgrs111033433
Max Magnitude0
ClinVar
Risk rs111033433(;)
Alt rs111033433(;)
Reference rs111033433(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76894154delC
CLNSRC ClinVar
CLNACC RCV000036106.2,