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rs111033192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033192(A;A)
Make rs111033192(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77207370
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033192
ebirs111033192
HLIrs111033192
Exacrs111033192
Varsomers111033192
Maprs111033192
PheGenIrs111033192
hapmaprs111033192
1000 genomesrs111033192
hgdprs111033192
ensemblrs111033192
gopubmedrs111033192
geneviewrs111033192
scholarrs111033192
googlers111033192
pharmgkbrs111033192
gwascentralrs111033192
openSNPrs111033192
23andMers111033192
23andMe allrs111033192
SNP Nexus

SNPshotrs111033192
SNPdbers111033192
MSV3drs111033192
GWAS Ctlgrs111033192
Max Magnitude0
ClinVar
Risk rs111033192(A,T;A,T)
Alt rs111033192(A,T;A,T)
Reference rs111033192(G;G)
Significance Pathogenic
Disease not specified Usher syndrome
Variation info
Gene MYO7A
CLNDBN not specified Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76918415G>A; NC_000011.9:g.76918415G>T
CLNSRC ClinVar
CLNACC RCV000036204.2, RCV000036205.2,