rs1777672
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs1777672(C;C) |
Make rs1777672(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 35603682 |
Gene | NBEA |
is a | snp |
is | mentioned by |
dbSNP | rs1777672 |
dbSNP (classic) | rs1777672 |
ClinGen | rs1777672 |
ebi | rs1777672 |
HLI | rs1777672 |
Exac | rs1777672 |
Gnomad | rs1777672 |
Varsome | rs1777672 |
LitVar | rs1777672 |
Map | rs1777672 |
PheGenI | rs1777672 |
Biobank | rs1777672 |
1000 genomes | rs1777672 |
hgdp | rs1777672 |
ensembl | rs1777672 |
geneview | rs1777672 |
scholar | rs1777672 |
rs1777672 | |
pharmgkb | rs1777672 |
gwascentral | rs1777672 |
openSNP | rs1777672 |
23andMe | rs1777672 |
SNPshot | rs1777672 |
SNPdbe | rs1777672 |
MSV3d | rs1777672 |
GWAS Ctlg | rs1777672 |
GMAF | 0.04683 |
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 | 4E-7 |
Odds Ratio | NR NR |