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rs111033239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033239(-;-)
Make rs111033239(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77189372
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033239
ebirs111033239
HLIrs111033239
Exacrs111033239
Varsomers111033239
Maprs111033239
PheGenIrs111033239
hapmaprs111033239
1000 genomesrs111033239
hgdprs111033239
ensemblrs111033239
gopubmedrs111033239
geneviewrs111033239
scholarrs111033239
googlers111033239
pharmgkbrs111033239
gwascentralrs111033239
openSNPrs111033239
23andMers111033239
23andMe allrs111033239
SNP Nexus

SNPshotrs111033239
SNPdbers111033239
MSV3drs111033239
GWAS Ctlgrs111033239
Max Magnitude0
ClinVar
Risk rs111033239(;)
Alt rs111033239(;)
Reference rs111033239(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76900417delC
CLNSRC ClinVar
CLNACC RCV000036113.2,