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rs111033428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGTCCTATTAT;GGTCCTATTAT) 0 common in clinvar
Make rs111033428(-;-)
Make rs111033428(-;GGTCCTATTAT)
ReferenceGRCh38 38.1/141
Chromosome1
Position215782187
GeneUSH2A
is asnp
is mentioned by
dbSNPrs111033428
ebirs111033428
HLIrs111033428
Exacrs111033428
Varsomers111033428
Maprs111033428
PheGenIrs111033428
hapmaprs111033428
1000 genomesrs111033428
hgdprs111033428
ensemblrs111033428
gopubmedrs111033428
geneviewrs111033428
scholarrs111033428
googlers111033428
pharmgkbrs111033428
gwascentralrs111033428
openSNPrs111033428
23andMers111033428
23andMe allrs111033428
SNP Nexus

SNPshotrs111033428
SNPdbers111033428
MSV3drs111033428
GWAS Ctlgrs111033428
Max Magnitude0
ClinVar
Risk rs111033428(;)
Alt rs111033428(;)
Reference rs111033428(GGTCCTATTAT;GGTCCTATTAT)
Significance Untested
Disease
Variation info
Gene USH2A
CLNDBN
Reversed 1
HGVS NC_000001.10:g.215955529_215955539delATAATAGGACCins13
CLNSRC
CLNACC