rs41386349
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs41386349(C;C) |
Make rs41386349(C;T) |
Make rs41386349(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 241851697 |
Gene | LOC105373977, PDCD1 |
is a | snp |
is | mentioned by |
dbSNP | rs41386349 |
dbSNP (classic) | rs41386349 |
ClinGen | rs41386349 |
ebi | rs41386349 |
HLI | rs41386349 |
Exac | rs41386349 |
Gnomad | rs41386349 |
Varsome | rs41386349 |
LitVar | rs41386349 |
Map | rs41386349 |
PheGenI | rs41386349 |
Biobank | rs41386349 |
1000 genomes | rs41386349 |
hgdp | rs41386349 |
ensembl | rs41386349 |
geneview | rs41386349 |
scholar | rs41386349 |
rs41386349 | |
pharmgkb | rs41386349 |
gwascentral | rs41386349 |
openSNP | rs41386349 |
23andMe | rs41386349 |
SNPshot | rs41386349 |
SNPdbe | rs41386349 |
MSV3d | rs41386349 |
GWAS Ctlg | rs41386349 |
GMAF | 0.1598 |
Max Magnitude | 0 |
[PMID 19468750] Programmed death-1 (PD-1) gene polymorphisms lodged in the genetic predispositions of Kawasaki Disease
[PMID 23628397] Lack of association between CTLA-4 and PDCD1 polymorphisms and acute rejection in German liver transplant recipients
[PMID 31464942] Association of rs10204525 genotype GG and rs2227982 CC combination in programmed cell death 1 with hepatitis B virus infection risk.