rs8001611
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8001611(C;C) |
Make rs8001611(C;T) |
Make rs8001611(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 13 |
Position | 42391558 |
is a | snp |
is | mentioned by |
dbSNP | rs8001611 |
dbSNP (classic) | rs8001611 |
ClinGen | rs8001611 |
ebi | rs8001611 |
HLI | rs8001611 |
Exac | rs8001611 |
Gnomad | rs8001611 |
Varsome | rs8001611 |
LitVar | rs8001611 |
Map | rs8001611 |
PheGenI | rs8001611 |
Biobank | rs8001611 |
1000 genomes | rs8001611 |
hgdp | rs8001611 |
ensembl | rs8001611 |
geneview | rs8001611 |
scholar | rs8001611 |
rs8001611 | |
pharmgkb | rs8001611 |
gwascentral | rs8001611 |
openSNP | rs8001611 |
23andMe | rs8001611 |
SNPshot | rs8001611 |
SNPdbe | rs8001611 |
MSV3d | rs8001611 |
GWAS Ctlg | rs8001611 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23644456] |
Trait | Bone mineral density |
Title | Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits. |
Risk Allele | |
P-val | 2E-12 |
Odds Ratio | 1.21 [NR] |