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rs111033276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs111033276(-;-)
Make rs111033276(-;C)
Make rs111033276(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77203099
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033276
ebirs111033276
HLIrs111033276
Exacrs111033276
Varsomers111033276
Maprs111033276
PheGenIrs111033276
hapmaprs111033276
1000 genomesrs111033276
hgdprs111033276
ensemblrs111033276
gopubmedrs111033276
geneviewrs111033276
scholarrs111033276
googlers111033276
pharmgkbrs111033276
gwascentralrs111033276
openSNPrs111033276
23andMers111033276
23andMe allrs111033276
SNP Nexus

SNPshotrs111033276
SNPdbers111033276
MSV3drs111033276
GWAS Ctlgrs111033276
Max Magnitude0
ClinVar
Risk rs111033276(C;C)
Alt rs111033276(C;C)
Reference rs111033276(;)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76914144dupC
CLNSRC ClinVar
CLNACC RCV000036180.2,