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rs111033404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033404(C;C)
Make rs111033404(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77174915
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033404
ebirs111033404
HLIrs111033404
Exacrs111033404
Varsomers111033404
Maprs111033404
PheGenIrs111033404
hapmaprs111033404
1000 genomesrs111033404
hgdprs111033404
ensemblrs111033404
gopubmedrs111033404
geneviewrs111033404
scholarrs111033404
googlers111033404
pharmgkbrs111033404
gwascentralrs111033404
openSNPrs111033404
23andMers111033404
23andMe allrs111033404
SNP Nexus

SNPshotrs111033404
SNPdbers111033404
MSV3drs111033404
GWAS Ctlgrs111033404
Max Magnitude0
ClinVar
Risk rs111033404(A,C;A,C)
Alt rs111033404(A,C;A,C)
Reference rs111033404(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76885961G>A; NC_000011.9:g.76885961G>C
CLNSRC ClinVar
CLNACC RCV000036075.2, RCV000036076.2,