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rs3917657

From SNPedia

Orientationminus
Stabilizedminus
Make rs3917657(C;C)
Make rs3917657(C;T)
Make rs3917657(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169629504
GeneSELP
is asnp
is mentioned by
dbSNPrs3917657
ebirs3917657
HLIrs3917657
Exacrs3917657
Varsomers3917657
Maprs3917657
PheGenIrs3917657
hapmaprs3917657
1000 genomesrs3917657
hgdprs3917657
ensemblrs3917657
gopubmedrs3917657
geneviewrs3917657
scholarrs3917657
googlers3917657
pharmgkbrs3917657
gwascentralrs3917657
openSNPrs3917657
23andMers3917657
23andMe allrs3917657
SNP Nexus

SNPshotrs3917657
SNPdbers3917657
MSV3drs3917657
GWAS Ctlgrs3917657
GMAF0.1125
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