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rs111033337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033337(A;C)
Make rs111033337(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77198493
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033337
ebirs111033337
HLIrs111033337
Exacrs111033337
Varsomers111033337
Maprs111033337
PheGenIrs111033337
hapmaprs111033337
1000 genomesrs111033337
hgdprs111033337
ensemblrs111033337
gopubmedrs111033337
geneviewrs111033337
scholarrs111033337
googlers111033337
pharmgkbrs111033337
gwascentralrs111033337
openSNPrs111033337
23andMers111033337
23andMe allrs111033337
SNP Nexus

SNPshotrs111033337
SNPdbers111033337
MSV3drs111033337
GWAS Ctlgrs111033337
Max Magnitude0
ClinVar
Risk rs111033337(C;C)
Alt rs111033337(C;C)
Reference rs111033337(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76909538A>C
CLNSRC ClinVar
CLNACC RCV000036144.2,