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rs1800807

From SNPedia

Orientationminus
Stabilizedminus
Make rs1800807(C;C)
Make rs1800807(C;G)
Make rs1800807(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169632197
is asnp
is mentioned by
dbSNPrs1800807
ebirs1800807
HLIrs1800807
Exacrs1800807
Varsomers1800807
Maprs1800807
PheGenIrs1800807
hapmaprs1800807
1000 genomesrs1800807
hgdprs1800807
ensemblrs1800807
gopubmedrs1800807
geneviewrs1800807
scholarrs1800807
googlers1800807
pharmgkbrs1800807
gwascentralrs1800807
openSNPrs1800807
23andMers1800807
23andMe allrs1800807
SNP Nexus

SNPshotrs1800807
SNPdbers1800807
MSV3drs1800807
GWAS Ctlgrs1800807
GMAF0.4835
Max Magnitude

[PMID 24504449] SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis [PMID 22192915] Common polymorphisms in the P-selectin gene in women with recurrent spontaneous abortions.