rs1385351
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1385351(C;C) |
Make rs1385351(C;T) |
Make rs1385351(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 192469177 |
is a | snp |
is | mentioned by |
dbSNP | rs1385351 |
dbSNP (classic) | rs1385351 |
ClinGen | rs1385351 |
ebi | rs1385351 |
HLI | rs1385351 |
Exac | rs1385351 |
Gnomad | rs1385351 |
Varsome | rs1385351 |
LitVar | rs1385351 |
Map | rs1385351 |
PheGenI | rs1385351 |
Biobank | rs1385351 |
1000 genomes | rs1385351 |
hgdp | rs1385351 |
ensembl | rs1385351 |
geneview | rs1385351 |
scholar | rs1385351 |
rs1385351 | |
pharmgkb | rs1385351 |
gwascentral | rs1385351 |
openSNP | rs1385351 |
23andMe | rs1385351 |
SNPshot | rs1385351 |
SNPdbe | rs1385351 |
MSV3d | rs1385351 |
GWAS Ctlg | rs1385351 |
GMAF | 0.2612 |
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 |