rs3795958
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs3795958(A;G) |
Make rs3795958(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 26444262 |
Gene | DRC1 |
is a | snp |
is | mentioned by |
dbSNP | rs3795958 |
dbSNP (classic) | rs3795958 |
ClinGen | rs3795958 |
ebi | rs3795958 |
HLI | rs3795958 |
Exac | rs3795958 |
Gnomad | rs3795958 |
Varsome | rs3795958 |
LitVar | rs3795958 |
Map | rs3795958 |
PheGenI | rs3795958 |
Biobank | rs3795958 |
1000 genomes | rs3795958 |
hgdp | rs3795958 |
ensembl | rs3795958 |
geneview | rs3795958 |
scholar | rs3795958 |
rs3795958 | |
pharmgkb | rs3795958 |
gwascentral | rs3795958 |
openSNP | rs3795958 |
23andMe | rs3795958 |
SNPshot | rs3795958 |
SNPdbe | rs3795958 |
MSV3d | rs3795958 |
GWAS Ctlg | rs3795958 |
GMAF | 0.1584 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23319000] |
Trait | Metabolite levels (HVA) |
Title | Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. |
Risk Allele | G |
P-val | 2E-6 |
Odds Ratio | .24 unit increase |
ClinVar | |
---|---|
Risk | rs3795958(G;G) |
Alt | rs3795958(G;G) |
Reference | Rs3795958(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | DRC1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.26667130A>G |
CLNSRC | |
CLNACC | RCV000454516.1, |