rs16948255
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs16948255(C;T) |
Make rs16948255(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 74847922 |
is a | snp |
is | mentioned by |
dbSNP | rs16948255 |
dbSNP (classic) | rs16948255 |
ClinGen | rs16948255 |
ebi | rs16948255 |
HLI | rs16948255 |
Exac | rs16948255 |
Gnomad | rs16948255 |
Varsome | rs16948255 |
LitVar | rs16948255 |
Map | rs16948255 |
PheGenI | rs16948255 |
Biobank | rs16948255 |
1000 genomes | rs16948255 |
hgdp | rs16948255 |
ensembl | rs16948255 |
geneview | rs16948255 |
scholar | rs16948255 |
rs16948255 | |
pharmgkb | rs16948255 |
gwascentral | rs16948255 |
openSNP | rs16948255 |
23andMe | rs16948255 |
SNPshot | rs16948255 |
SNPdbe | rs16948255 |
MSV3d | rs16948255 |
GWAS Ctlg | rs16948255 |
GMAF | 0.02847 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20041166] |
Trait | HIV-1 control |
Title | Common Genetic Variation and the Control of HIV-1 in Human |
Risk Allele | |
P-val | 0.000001 |
Odds Ratio | NR NR |