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rs111033587

From SNPedia

Merged intors35315638
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033587(G;G)
Make rs111033587(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249796
GeneHBG1
is asnp
is mentioned by
dbSNPrs111033587
ebirs111033587
HLIrs111033587
Exacrs111033587
Varsomers111033587
Maprs111033587
PheGenIrs111033587
hapmaprs111033587
1000 genomesrs111033587
hgdprs111033587
ensemblrs111033587
gopubmedrs111033587
geneviewrs111033587
scholarrs111033587
googlers111033587
pharmgkbrs111033587
gwascentralrs111033587
openSNPrs111033587
23andMers111033587
23andMe allrs111033587
SNP Nexus

SNPshotrs111033587
SNPdbers111033587
MSV3drs111033587
GWAS Ctlgrs111033587
StatusMerged into rs35315638
Max Magnitude0
OMIM142200
Desc
Variant0035
Relatedalso
ClinVar
Risk rs111033587(G;G)
Alt rs111033587(G;G)
Reference rs111033587(T;T)
Significance Untested
Disease
Variation info
Gene HBG1
CLNDBN
Reversed 1
HGVS NC_000011.9:g.5271026A>C
CLNSRC
CLNACC