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rs111033386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033386(A;A)
Make rs111033386(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position216046532
GeneUSH2A
is asnp
is mentioned by
dbSNPrs111033386
ebirs111033386
HLIrs111033386
Exacrs111033386
Varsomers111033386
Maprs111033386
PheGenIrs111033386
hapmaprs111033386
1000 genomesrs111033386
hgdprs111033386
ensemblrs111033386
gopubmedrs111033386
geneviewrs111033386
scholarrs111033386
googlers111033386
pharmgkbrs111033386
gwascentralrs111033386
openSNPrs111033386
23andMers111033386
23andMe allrs111033386
SNP Nexus

SNPshotrs111033386
SNPdbers111033386
MSV3drs111033386
GWAS Ctlgrs111033386
Max Magnitude0
ClinVar
Risk rs111033386(A;A)
Alt rs111033386(A;A)
Reference rs111033386(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.216219874C>T
CLNSRC ClinVar
CLNACC RCV000041880.2,