Have questions? Visit https://www.reddit.com/r/SNPedia

rs111033529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033529(A;A)
Make rs111033529(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position215878891
GeneUSH2A
is asnp
is mentioned by
dbSNPrs111033529
ebirs111033529
HLIrs111033529
Exacrs111033529
Varsomers111033529
Maprs111033529
PheGenIrs111033529
hapmaprs111033529
1000 genomesrs111033529
hgdprs111033529
ensemblrs111033529
gopubmedrs111033529
geneviewrs111033529
scholarrs111033529
googlers111033529
pharmgkbrs111033529
gwascentralrs111033529
openSNPrs111033529
23andMers111033529
23andMe allrs111033529
SNP Nexus

SNPshotrs111033529
SNPdbers111033529
MSV3drs111033529
GWAS Ctlgrs111033529
Max Magnitude0
ClinVar
Risk rs111033529(A;A)
Alt rs111033529(A;A)
Reference rs111033529(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene USH2A
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.216052233G>T
CLNSRC ClinVar
CLNACC RCV000041927.3,