rs2407103
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2407103(A;A) |
Make rs2407103(A;G) |
Make rs2407103(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 37094396 |
Gene | LOC642879 |
is a | snp |
is | mentioned by |
dbSNP | rs2407103 |
dbSNP (classic) | rs2407103 |
ClinGen | rs2407103 |
ebi | rs2407103 |
HLI | rs2407103 |
Exac | rs2407103 |
Gnomad | rs2407103 |
Varsome | rs2407103 |
LitVar | rs2407103 |
Map | rs2407103 |
PheGenI | rs2407103 |
Biobank | rs2407103 |
1000 genomes | rs2407103 |
hgdp | rs2407103 |
ensembl | rs2407103 |
geneview | rs2407103 |
scholar | rs2407103 |
rs2407103 | |
pharmgkb | rs2407103 |
gwascentral | rs2407103 |
openSNP | rs2407103 |
23andMe | rs2407103 |
SNPshot | rs2407103 |
SNPdbe | rs2407103 |
MSV3d | rs2407103 |
GWAS Ctlg | rs2407103 |
GMAF | 0.1327 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21901158] |
Trait | |
Title | Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study. |
Risk Allele | C |
P-val | 0.000002 |
Odds Ratio | 15.0000 [9.00 - 23.00] % increase |