rs2071566
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2071566(A;A) |
Make rs2071566(A;G) |
Make rs2071566(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 64940282 |
Gene | CHURC1-FNTB, GPX2 |
is a | snp |
is | mentioned by |
dbSNP | rs2071566 |
dbSNP (classic) | rs2071566 |
ClinGen | rs2071566 |
ebi | rs2071566 |
HLI | rs2071566 |
Exac | rs2071566 |
Gnomad | rs2071566 |
Varsome | rs2071566 |
LitVar | rs2071566 |
Map | rs2071566 |
PheGenI | rs2071566 |
Biobank | rs2071566 |
1000 genomes | rs2071566 |
hgdp | rs2071566 |
ensembl | rs2071566 |
geneview | rs2071566 |
scholar | rs2071566 |
rs2071566 | |
pharmgkb | rs2071566 |
gwascentral | rs2071566 |
openSNP | rs2071566 |
23andMe | rs2071566 |
SNPshot | rs2071566 |
SNPdbe | rs2071566 |
MSV3d | rs2071566 |
GWAS Ctlg | rs2071566 |
GMAF | 0.4472 |
Max Magnitude | 0 |
[PMID 22259188] Genetic Variation in GPX1 Is Associated with GPX1 Activity in a Comprehensive Analysis of Genetic Variations in Selenoenzyme Genes and Their Activity and Oxidative Stress in Humans