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rs111033215

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033215(A;A)
Make rs111033215(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77206108
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033215
ebirs111033215
HLIrs111033215
Exacrs111033215
Varsomers111033215
Maprs111033215
PheGenIrs111033215
hapmaprs111033215
1000 genomesrs111033215
hgdprs111033215
ensemblrs111033215
gopubmedrs111033215
geneviewrs111033215
scholarrs111033215
googlers111033215
pharmgkbrs111033215
gwascentralrs111033215
openSNPrs111033215
23andMers111033215
23andMe allrs111033215
SNP Nexus

SNPshotrs111033215
SNPdbers111033215
MSV3drs111033215
GWAS Ctlgrs111033215
Max Magnitude0
ClinVar
Risk rs111033215(A;A)
Alt rs111033215(A;A)
Reference rs111033215(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76917153G>A
CLNSRC
CLNACC RCV000036199.3,