rs78640361
From SNPedia
Merged into | rs223320 |
Orientation | plus |
Stabilized | plus |
Make rs78640361(A;A) |
Make rs78640361(A;T) |
Make rs78640361(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 102881008 |
Gene | CISD2 |
is a | snp |
is | mentioned by |
dbSNP | rs78640361 |
dbSNP (classic) | rs78640361 |
ClinGen | rs78640361 |
ebi | rs78640361 |
HLI | rs78640361 |
Exac | rs78640361 |
Gnomad | rs78640361 |
Varsome | rs78640361 |
LitVar | rs78640361 |
Map | rs78640361 |
PheGenI | rs78640361 |
Biobank | rs78640361 |
1000 genomes | rs78640361 |
hgdp | rs78640361 |
ensembl | rs78640361 |
geneview | rs78640361 |
scholar | rs78640361 |
rs78640361 | |
pharmgkb | rs78640361 |
gwascentral | rs78640361 |
openSNP | rs78640361 |
23andMe | rs78640361 |
SNPshot | rs78640361 |
SNPdbe | rs78640361 |
MSV3d | rs78640361 |
GWAS Ctlg | rs78640361 |
Status | Merged into rs223320 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24159190] |
Trait | Serum dimethylarginine levels (asymmetric) |
Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
Risk Allele | T |
P-val | 1E-6 |
Odds Ratio | .13 [0.076-0.178] unit decrease |