rs2204037
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2204037(C;C) |
Make rs2204037(C;T) |
Make rs2204037(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 62862667 |
Gene | LOC105370233 |
is a | snp |
is | mentioned by |
dbSNP | rs2204037 |
dbSNP (classic) | rs2204037 |
ClinGen | rs2204037 |
ebi | rs2204037 |
HLI | rs2204037 |
Exac | rs2204037 |
Gnomad | rs2204037 |
Varsome | rs2204037 |
LitVar | rs2204037 |
Map | rs2204037 |
PheGenI | rs2204037 |
Biobank | rs2204037 |
1000 genomes | rs2204037 |
hgdp | rs2204037 |
ensembl | rs2204037 |
geneview | rs2204037 |
scholar | rs2204037 |
rs2204037 | |
pharmgkb | rs2204037 |
gwascentral | rs2204037 |
openSNP | rs2204037 |
23andMe | rs2204037 |
SNPshot | rs2204037 |
SNPdbe | rs2204037 |
MSV3d | rs2204037 |
GWAS Ctlg | rs2204037 |
GMAF | 0.2934 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 5E-7 |
Odds Ratio | 1.38 [0.85-1.91] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 13
- 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 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d