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rs2217332

From SNPedia

Orientationminus
Stabilizedplus
Make rs2217332(C;C)
Make rs2217332(C;T)
Make rs2217332(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position56935236
GeneHERPUD1
is asnp
is mentioned by
dbSNPrs2217332
ebirs2217332
HLIrs2217332
Exacrs2217332
Varsomers2217332
Maprs2217332
PheGenIrs2217332
hapmaprs2217332
1000 genomesrs2217332
hgdprs2217332
ensemblrs2217332
gopubmedrs2217332
geneviewrs2217332
scholarrs2217332
googlers2217332
pharmgkbrs2217332
gwascentralrs2217332
openSNPrs2217332
23andMers2217332
23andMe allrs2217332
SNP Nexus

SNPshotrs2217332
SNPdbers2217332
MSV3drs2217332
GWAS Ctlgrs2217332
GMAF0.1166
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20694148OA-icon.png]
Trait
Title A genome-wide association study of the metabolic syndrome in Indian Asian men
Risk Allele
P-val 0.000003
Odds Ratio None None

[PMID 20031564OA-icon.png] Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.


GET Evidence
HERPUD1-R50H
aa_change Arg50His
aa_change_short R50H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.149563
summary



[PMID 26823705] Evidence of a novel gene HERPUD1 in polypoidal choroidal vasculopathy.