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rs111033390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs111033390(-;-)
Make rs111033390(-;CA)
Make rs111033390(CA;CA)
ReferenceGRCh38 38.1/141
Chromosome11
Position77189384
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033390
ebirs111033390
HLIrs111033390
Exacrs111033390
Varsomers111033390
Maprs111033390
PheGenIrs111033390
hapmaprs111033390
1000 genomesrs111033390
hgdprs111033390
ensemblrs111033390
gopubmedrs111033390
geneviewrs111033390
scholarrs111033390
googlers111033390
pharmgkbrs111033390
gwascentralrs111033390
openSNPrs111033390
23andMers111033390
23andMe allrs111033390
SNP Nexus

SNPshotrs111033390
SNPdbers111033390
MSV3drs111033390
GWAS Ctlgrs111033390
Max Magnitude0
ClinVar
Risk rs111033390(CA;CA)
Alt rs111033390(CA;CA)
Reference rs111033390(;)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76900428_76900429dupCA
CLNSRC ClinVar
CLNACC RCV000036115.2,