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rs3917687

From SNPedia

Orientationminus
Stabilizedplus
Make rs3917687(C;C)
Make rs3917687(C;T)
Make rs3917687(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position169621855
GeneSELP
is asnp
is mentioned by
dbSNPrs3917687
ebirs3917687
HLIrs3917687
Exacrs3917687
Varsomers3917687
Maprs3917687
PheGenIrs3917687
hapmaprs3917687
1000 genomesrs3917687
hgdprs3917687
ensemblrs3917687
gopubmedrs3917687
geneviewrs3917687
scholarrs3917687
googlers3917687
pharmgkbrs3917687
gwascentralrs3917687
openSNPrs3917687
23andMers3917687
23andMe allrs3917687
SNP Nexus

SNPshotrs3917687
SNPdbers3917687
MSV3drs3917687
GWAS Ctlgrs3917687
GMAF0.1304
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19404301OA-icon.png] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE