rs2239774
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs2239774(C;C) |
Make rs2239774(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 37241613 |
Gene | RAC2 |
is a | snp |
is | mentioned by |
dbSNP | rs2239774 |
dbSNP (classic) | rs2239774 |
ClinGen | rs2239774 |
ebi | rs2239774 |
HLI | rs2239774 |
Exac | rs2239774 |
Gnomad | rs2239774 |
Varsome | rs2239774 |
LitVar | rs2239774 |
Map | rs2239774 |
PheGenI | rs2239774 |
Biobank | rs2239774 |
1000 genomes | rs2239774 |
hgdp | rs2239774 |
ensembl | rs2239774 |
geneview | rs2239774 |
scholar | rs2239774 |
rs2239774 | |
pharmgkb | rs2239774 |
gwascentral | rs2239774 |
openSNP | rs2239774 |
23andMe | rs2239774 |
SNPshot | rs2239774 |
SNPdbe | rs2239774 |
MSV3d | rs2239774 |
GWAS Ctlg | rs2239774 |
GMAF | 0.169 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 19505917] Lead exposure, polymorphisms in genes related to oxidative stress, and risk of adult brain tumors
ClinVar | |
---|---|
Risk | rs2239774(C;C) |
Alt | rs2239774(C;C) |
Reference | Rs2239774(G;G) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | RAC2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000022.10:g.37637653G>C |
CLNSRC | ClinVar GeneDx |
CLNACC | RCV000127684.1, |