rs4715291
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4715291(C;C) |
Make rs4715291(C;T) |
Make rs4715291(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 52248562 |
is a | snp |
is | mentioned by |
dbSNP | rs4715291 |
dbSNP (classic) | rs4715291 |
ClinGen | rs4715291 |
ebi | rs4715291 |
HLI | rs4715291 |
Exac | rs4715291 |
Gnomad | rs4715291 |
Varsome | rs4715291 |
LitVar | rs4715291 |
Map | rs4715291 |
PheGenI | rs4715291 |
Biobank | rs4715291 |
1000 genomes | rs4715291 |
hgdp | rs4715291 |
ensembl | rs4715291 |
geneview | rs4715291 |
scholar | rs4715291 |
rs4715291 | |
pharmgkb | rs4715291 |
gwascentral | rs4715291 |
openSNP | rs4715291 |
23andMe | rs4715291 |
SNPshot | rs4715291 |
SNPdbe | rs4715291 |
MSV3d | rs4715291 |
GWAS Ctlg | rs4715291 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26667835] IL17F and IL17RA genetic variants increase risk of cerebral malaria in two African populations.