rs3753306
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3753306(C;C) |
Make rs3753306(C;T) |
Make rs3753306(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 169630994 |
Gene | SELP |
is a | snp |
is | mentioned by |
dbSNP | rs3753306 |
dbSNP (classic) | rs3753306 |
ClinGen | rs3753306 |
ebi | rs3753306 |
HLI | rs3753306 |
Exac | rs3753306 |
Gnomad | rs3753306 |
Varsome | rs3753306 |
LitVar | rs3753306 |
Map | rs3753306 |
PheGenI | rs3753306 |
Biobank | rs3753306 |
1000 genomes | rs3753306 |
hgdp | rs3753306 |
ensembl | rs3753306 |
geneview | rs3753306 |
scholar | rs3753306 |
rs3753306 | |
pharmgkb | rs3753306 |
gwascentral | rs3753306 |
openSNP | rs3753306 |
23andMe | rs3753306 |
SNPshot | rs3753306 |
SNPdbe | rs3753306 |
MSV3d | rs3753306 |
GWAS Ctlg | rs3753306 |
GMAF | 0.2374 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19404301] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE
[PMID 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.