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rs3917751

From SNPedia

Orientationminus
Stabilizedminus
Make rs3917751(C;C)
Make rs3917751(C;T)
Make rs3917751(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169607330
GeneSELP
is asnp
is mentioned by
dbSNPrs3917751
ebirs3917751
HLIrs3917751
Exacrs3917751
Varsomers3917751
Maprs3917751
PheGenIrs3917751
hapmaprs3917751
1000 genomesrs3917751
hgdprs3917751
ensemblrs3917751
gopubmedrs3917751
geneviewrs3917751
scholarrs3917751
googlers3917751
pharmgkbrs3917751
gwascentralrs3917751
openSNPrs3917751
23andMers3917751
23andMe allrs3917751
SNP Nexus

SNPshotrs3917751
SNPdbers3917751
MSV3drs3917751
GWAS Ctlgrs3917751
GMAF0.4991
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21521525OA-icon.png] Evaluation of variants in the selectin genes in age-related macular degeneration

[PMID 19404301OA-icon.png] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.