rs17027625
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs17027625(C;C) |
Make rs17027625(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 31404088 |
Gene | THRAP3P1 |
is a | snp |
is | mentioned by |
dbSNP | rs17027625 |
dbSNP (classic) | rs17027625 |
ClinGen | rs17027625 |
ebi | rs17027625 |
HLI | rs17027625 |
Exac | rs17027625 |
Gnomad | rs17027625 |
Varsome | rs17027625 |
LitVar | rs17027625 |
Map | rs17027625 |
PheGenI | rs17027625 |
Biobank | rs17027625 |
1000 genomes | rs17027625 |
hgdp | rs17027625 |
ensembl | rs17027625 |
geneview | rs17027625 |
scholar | rs17027625 |
rs17027625 | |
pharmgkb | rs17027625 |
gwascentral | rs17027625 |
openSNP | rs17027625 |
23andMe | rs17027625 |
SNPshot | rs17027625 |
SNPdbe | rs17027625 |
MSV3d | rs17027625 |
GWAS Ctlg | rs17027625 |
GMAF | 0.03627 |
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 | 0.000004 |
Odds Ratio | NR NR |
[PMID 20823317] is-rSNP: a novel technique for in silico regulatory SNP detection.