rs3103778
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3103778(A;A) |
Make rs3103778(A;G) |
Make rs3103778(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 39968099 |
Gene | MFSD2A |
is a | snp |
is | mentioned by |
dbSNP | rs3103778 |
dbSNP (classic) | rs3103778 |
ClinGen | rs3103778 |
ebi | rs3103778 |
HLI | rs3103778 |
Exac | rs3103778 |
Gnomad | rs3103778 |
Varsome | rs3103778 |
LitVar | rs3103778 |
Map | rs3103778 |
PheGenI | rs3103778 |
Biobank | rs3103778 |
1000 genomes | rs3103778 |
hgdp | rs3103778 |
ensembl | rs3103778 |
geneview | rs3103778 |
scholar | rs3103778 |
rs3103778 | |
pharmgkb | rs3103778 |
gwascentral | rs3103778 |
openSNP | rs3103778 |
23andMe | rs3103778 |
SNPshot | rs3103778 |
SNPdbe | rs3103778 |
MSV3d | rs3103778 |
GWAS Ctlg | rs3103778 |
GMAF | 0.4761 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23534349] |
Trait | PR interval |
Title | Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans. |
Risk Allele | G |
P-val | 9E-6 |
Odds Ratio | 6.30 [NR] ms increase |