rs7905537
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7905537(A;A) |
Make rs7905537(A;C) |
Make rs7905537(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 33942347 |
is a | snp |
is | mentioned by |
dbSNP | rs7905537 |
dbSNP (classic) | rs7905537 |
ClinGen | rs7905537 |
ebi | rs7905537 |
HLI | rs7905537 |
Exac | rs7905537 |
Gnomad | rs7905537 |
Varsome | rs7905537 |
LitVar | rs7905537 |
Map | rs7905537 |
PheGenI | rs7905537 |
Biobank | rs7905537 |
1000 genomes | rs7905537 |
hgdp | rs7905537 |
ensembl | rs7905537 |
geneview | rs7905537 |
scholar | rs7905537 |
rs7905537 | |
pharmgkb | rs7905537 |
gwascentral | rs7905537 |
openSNP | rs7905537 |
23andMe | rs7905537 |
SNPshot | rs7905537 |
SNPdbe | rs7905537 |
MSV3d | rs7905537 |
GWAS Ctlg | rs7905537 |
GMAF | 0.2461 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20709820] |
Trait | |
Title | Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema |
Risk Allele | A |
P-val | 8E-7 |
Odds Ratio | 1.85 [NR] HU increase |