rs3917751
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3917751(C;C) |
Make rs3917751(C;T) |
Make rs3917751(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 169607330 |
Gene | SELP |
is a | snp |
is | mentioned by |
dbSNP | rs3917751 |
dbSNP (classic) | rs3917751 |
ClinGen | rs3917751 |
ebi | rs3917751 |
HLI | rs3917751 |
Exac | rs3917751 |
Gnomad | rs3917751 |
Varsome | rs3917751 |
LitVar | rs3917751 |
Map | rs3917751 |
PheGenI | rs3917751 |
Biobank | rs3917751 |
1000 genomes | rs3917751 |
hgdp | rs3917751 |
ensembl | rs3917751 |
geneview | rs3917751 |
scholar | rs3917751 |
rs3917751 | |
pharmgkb | rs3917751 |
gwascentral | rs3917751 |
openSNP | rs3917751 |
23andMe | rs3917751 |
SNPshot | rs3917751 |
SNPdbe | rs3917751 |
MSV3d | rs3917751 |
GWAS Ctlg | rs3917751 |
GMAF | 0.4991 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21521525] Evaluation of variants in the selectin genes in age-related macular degeneration
[PMID 19404301] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.