rs7698623
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs7698623(C;T) |
Make rs7698623(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 87834676 |
Gene | MEPE |
is a | snp |
is | mentioned by |
dbSNP | rs7698623 |
dbSNP (classic) | rs7698623 |
ClinGen | rs7698623 |
ebi | rs7698623 |
HLI | rs7698623 |
Exac | rs7698623 |
Gnomad | rs7698623 |
Varsome | rs7698623 |
LitVar | rs7698623 |
Map | rs7698623 |
PheGenI | rs7698623 |
Biobank | rs7698623 |
1000 genomes | rs7698623 |
hgdp | rs7698623 |
ensembl | rs7698623 |
geneview | rs7698623 |
scholar | rs7698623 |
rs7698623 | |
pharmgkb | rs7698623 |
gwascentral | rs7698623 |
openSNP | rs7698623 |
23andMe | rs7698623 |
SNPshot | rs7698623 |
SNPdbe | rs7698623 |
MSV3d | rs7698623 |
GWAS Ctlg | rs7698623 |
GMAF | 0.07622 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21779381] |
Trait | |
Title | Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study. |
Risk Allele | |
P-val | 3E-7 |
Odds Ratio | 6.3700 [3.15-12.90] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 4
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d