rs691005
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs691005(C;C) |
Make rs691005(C;T) |
Make rs691005(T;T) |
Reference | GRCh37 37.1/131 |
Chromosome | 10 |
Position | 17962845 |
is a | snp |
is | mentioned by |
dbSNP | rs691005 |
dbSNP (classic) | rs691005 |
ClinGen | rs691005 |
ebi | rs691005 |
HLI | rs691005 |
Exac | rs691005 |
Gnomad | rs691005 |
Varsome | rs691005 |
LitVar | rs691005 |
Map | rs691005 |
PheGenI | rs691005 |
Biobank | rs691005 |
1000 genomes | rs691005 |
hgdp | rs691005 |
ensembl | rs691005 |
geneview | rs691005 |
scholar | rs691005 |
rs691005 | |
pharmgkb | rs691005 |
gwascentral | rs691005 |
openSNP | rs691005 |
23andMe | rs691005 |
SNPshot | rs691005 |
SNPdbe | rs691005 |
MSV3d | rs691005 |
GWAS Ctlg | rs691005 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19902202] Genetic variants in the mannose receptor gene (MRC1) are associated with asthma in two independent populations
[PMID 21029423] Genetic variants in mannose receptor gene (MRC1) confer susceptibility to increased risk of sarcoidosis