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rs111033403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033403(A;A)
Make rs111033403(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77156018
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033403
ebirs111033403
HLIrs111033403
Exacrs111033403
Varsomers111033403
Maprs111033403
PheGenIrs111033403
hapmaprs111033403
1000 genomesrs111033403
hgdprs111033403
ensemblrs111033403
gopubmedrs111033403
geneviewrs111033403
scholarrs111033403
googlers111033403
pharmgkbrs111033403
gwascentralrs111033403
openSNPrs111033403
23andMers111033403
23andMe allrs111033403
SNP Nexus

SNPshotrs111033403
SNPdbers111033403
MSV3drs111033403
GWAS Ctlgrs111033403
Max Magnitude0
ClinVar
Risk rs111033403(A,T;A,T)
Alt rs111033403(A,T;A,T)
Reference rs111033403(C;C)
Significance Probable-Pathogenic
Disease not specified Usher syndrome
Variation info
Gene MYO7A
CLNDBN not specified Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76867064C>A; NC_000011.9:g.76867064C>T
CLNSRC ClinVar
CLNACC RCV000151476.1, RCV000036132.2,