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rs111033202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033202(-;-)
Make rs111033202(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77192191
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033202
ebirs111033202
HLIrs111033202
Exacrs111033202
Varsomers111033202
Maprs111033202
PheGenIrs111033202
hapmaprs111033202
1000 genomesrs111033202
hgdprs111033202
ensemblrs111033202
gopubmedrs111033202
geneviewrs111033202
scholarrs111033202
googlers111033202
pharmgkbrs111033202
gwascentralrs111033202
openSNPrs111033202
23andMers111033202
23andMe allrs111033202
SNP Nexus

SNPshotrs111033202
SNPdbers111033202
MSV3drs111033202
GWAS Ctlgrs111033202
Max Magnitude0
ClinVar
Risk rs111033202(;)
Alt rs111033202(;)
Reference rs111033202(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76903236delC
CLNSRC ClinVar
CLNACC RCV000036136.2,