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rs1800805

From SNPedia

Orientationminus
Stabilizedminus
Make rs1800805(A;A)
Make rs1800805(A;G)
Make rs1800805(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169632043
GeneSELP
is asnp
is mentioned by
dbSNPrs1800805
ebirs1800805
HLIrs1800805
Exacrs1800805
Varsomers1800805
Maprs1800805
PheGenIrs1800805
hapmaprs1800805
1000 genomesrs1800805
hgdprs1800805
ensemblrs1800805
gopubmedrs1800805
geneviewrs1800805
scholarrs1800805
googlers1800805
pharmgkbrs1800805
gwascentralrs1800805
openSNPrs1800805
23andMers1800805
23andMe allrs1800805
SNP Nexus

SNPshotrs1800805
SNPdbers1800805
MSV3drs1800805
GWAS Ctlgrs1800805
GMAF0.2608
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24504449] SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis


[PMID 16820586OA-icon.png] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.


[PMID 22192915] Common polymorphisms in the P-selectin gene in women with recurrent spontaneous abortions.