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rs111033426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033426(A;A)
Make rs111033426(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77142708
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033426
ebirs111033426
HLIrs111033426
Exacrs111033426
Varsomers111033426
Maprs111033426
PheGenIrs111033426
hapmaprs111033426
1000 genomesrs111033426
hgdprs111033426
ensemblrs111033426
gopubmedrs111033426
geneviewrs111033426
scholarrs111033426
googlers111033426
pharmgkbrs111033426
gwascentralrs111033426
openSNPrs111033426
23andMers111033426
23andMe allrs111033426
SNP Nexus

SNPshotrs111033426
SNPdbers111033426
MSV3drs111033426
GWAS Ctlgrs111033426
Max Magnitude0
ClinVar
Risk rs111033426(A;A)
Alt rs111033426(A;A)
Reference rs111033426(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76853754G>A
CLNSRC ClinVar
CLNACC RCV000036067.2,