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rs111033238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033238(-;-)
Make rs111033238(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77156771
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033238
ebirs111033238
HLIrs111033238
Exacrs111033238
Varsomers111033238
Maprs111033238
PheGenIrs111033238
hapmaprs111033238
1000 genomesrs111033238
hgdprs111033238
ensemblrs111033238
gopubmedrs111033238
geneviewrs111033238
scholarrs111033238
googlers111033238
pharmgkbrs111033238
gwascentralrs111033238
openSNPrs111033238
23andMers111033238
23andMe allrs111033238
SNP Nexus

SNPshotrs111033238
SNPdbers111033238
MSV3drs111033238
GWAS Ctlgrs111033238
Max Magnitude0
ClinVar
Risk rs111033238(;)
Alt rs111033238(;)
Reference rs111033238(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76867817delC
CLNSRC ClinVar
CLNACC RCV000036206.2,