rs7604827
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7604827(C;C) |
Make rs7604827(C;T) |
Make rs7604827(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 214477166 |
Gene | VWC2L |
is a | snp |
is | mentioned by |
dbSNP | rs7604827 |
dbSNP (classic) | rs7604827 |
ClinGen | rs7604827 |
ebi | rs7604827 |
HLI | rs7604827 |
Exac | rs7604827 |
Gnomad | rs7604827 |
Varsome | rs7604827 |
LitVar | rs7604827 |
Map | rs7604827 |
PheGenI | rs7604827 |
Biobank | rs7604827 |
1000 genomes | rs7604827 |
hgdp | rs7604827 |
ensembl | rs7604827 |
geneview | rs7604827 |
scholar | rs7604827 |
rs7604827 | |
pharmgkb | rs7604827 |
gwascentral | rs7604827 |
openSNP | rs7604827 |
23andMe | rs7604827 |
SNPshot | rs7604827 |
SNPdbe | rs7604827 |
MSV3d | rs7604827 |
GWAS Ctlg | rs7604827 |
GMAF | 0.1488 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | C |
P-val | 5E-6 |
Odds Ratio | 6.54 [NR] ms increase |