rs2721173
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2721173(A;A) |
Make rs2721173(A;G) |
Make rs2721173(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 144519045 |
Gene | LRRC14, RECQL4 |
is a | snp |
is | mentioned by |
dbSNP | rs2721173 |
dbSNP (classic) | rs2721173 |
ClinGen | rs2721173 |
ebi | rs2721173 |
HLI | rs2721173 |
Exac | rs2721173 |
Gnomad | rs2721173 |
Varsome | rs2721173 |
LitVar | rs2721173 |
Map | rs2721173 |
PheGenI | rs2721173 |
Biobank | rs2721173 |
1000 genomes | rs2721173 |
hgdp | rs2721173 |
ensembl | rs2721173 |
geneview | rs2721173 |
scholar | rs2721173 |
rs2721173 | |
pharmgkb | rs2721173 |
gwascentral | rs2721173 |
openSNP | rs2721173 |
23andMe | rs2721173 |
SNPshot | rs2721173 |
SNPdbe | rs2721173 |
MSV3d | rs2721173 |
GWAS Ctlg | rs2721173 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25201988] Common genetic variants associated with cognitive performance identified using the proxy-phenotype method