rs6751349
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6751349(A;A) |
Make rs6751349(A;C) |
Make rs6751349(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 45949823 |
Gene | PRKCE |
is a | snp |
is | mentioned by |
dbSNP | rs6751349 |
dbSNP (classic) | rs6751349 |
ClinGen | rs6751349 |
ebi | rs6751349 |
HLI | rs6751349 |
Exac | rs6751349 |
Gnomad | rs6751349 |
Varsome | rs6751349 |
LitVar | rs6751349 |
Map | rs6751349 |
PheGenI | rs6751349 |
Biobank | rs6751349 |
1000 genomes | rs6751349 |
hgdp | rs6751349 |
ensembl | rs6751349 |
geneview | rs6751349 |
scholar | rs6751349 |
rs6751349 | |
pharmgkb | rs6751349 |
gwascentral | rs6751349 |
openSNP | rs6751349 |
23andMe | rs6751349 |
SNPshot | rs6751349 |
SNPdbe | rs6751349 |
MSV3d | rs6751349 |
GWAS Ctlg | rs6751349 |
GMAF | 0.1483 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23166209] |
Trait | QT interval |
Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
Risk Allele | A |
P-val | 8E-6 |
Odds Ratio | 1.22 [0.69-1.75] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- 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