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rs111033510

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs111033510(-;-)
Make rs111033510(-;AG)
Make rs111033510(AG;AG)
ReferenceGRCh38 38.1/141
Chromosome11
Position77174772
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033510
ebirs111033510
HLIrs111033510
Exacrs111033510
Varsomers111033510
Maprs111033510
PheGenIrs111033510
hapmaprs111033510
1000 genomesrs111033510
hgdprs111033510
ensemblrs111033510
gopubmedrs111033510
geneviewrs111033510
scholarrs111033510
googlers111033510
pharmgkbrs111033510
gwascentralrs111033510
openSNPrs111033510
23andMers111033510
23andMe allrs111033510
SNP Nexus

SNPshotrs111033510
SNPdbers111033510
MSV3drs111033510
GWAS Ctlgrs111033510
Max Magnitude0
ClinVar
Risk rs111033510(AG;AG)
Alt rs111033510(AG;AG)
Reference rs111033510(;)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76885818_76885819insAG
CLNSRC ClinVar
CLNACC RCV000036069.2,