rs6128
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs6128(A;A) |
Make rs6128(A;G) |
Make rs6128(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 169593666 |
Gene | SELP |
is a | snp |
is | mentioned by |
dbSNP | rs6128 |
dbSNP (classic) | rs6128 |
ClinGen | rs6128 |
ebi | rs6128 |
HLI | rs6128 |
Exac | rs6128 |
Gnomad | rs6128 |
Varsome | rs6128 |
LitVar | rs6128 |
Map | rs6128 |
PheGenI | rs6128 |
Biobank | rs6128 |
1000 genomes | rs6128 |
hgdp | rs6128 |
ensembl | rs6128 |
geneview | rs6128 |
scholar | rs6128 |
rs6128 | |
pharmgkb | rs6128 |
gwascentral | rs6128 |
openSNP | rs6128 |
23andMe | rs6128 |
SNPshot | rs6128 |
SNPdbe | rs6128 |
MSV3d | rs6128 |
GWAS Ctlg | rs6128 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25794792] P-selectin plasma levels and genetic variant associated with diabetic retinopathy in African Americans
[PMID 26068646] The Functional Variant in the 3'UTR of IGF1 with the Risk of Gastric Cancer in a Chinese Population