rs309844
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs309844(C;C) |
Make rs309844(C;T) |
Make rs309844(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 29995847 |
is a | snp |
is | mentioned by |
dbSNP | rs309844 |
dbSNP (classic) | rs309844 |
ClinGen | rs309844 |
ebi | rs309844 |
HLI | rs309844 |
Exac | rs309844 |
Gnomad | rs309844 |
Varsome | rs309844 |
LitVar | rs309844 |
Map | rs309844 |
PheGenI | rs309844 |
Biobank | rs309844 |
1000 genomes | rs309844 |
hgdp | rs309844 |
ensembl | rs309844 |
geneview | rs309844 |
scholar | rs309844 |
rs309844 | |
pharmgkb | rs309844 |
gwascentral | rs309844 |
openSNP | rs309844 |
23andMe | rs309844 |
SNPshot | rs309844 |
SNPdbe | rs309844 |
MSV3d | rs309844 |
GWAS Ctlg | rs309844 |
GMAF | 0.1511 |
Max Magnitude | 0 |
[PMID 24322967] HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique