rs2232368
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2232368(A;A) |
Make rs2232368(A;G) |
Make rs2232368(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 49255822 |
Gene | FOXP3 |
is a | snp |
is | mentioned by |
dbSNP | rs2232368 |
dbSNP (classic) | rs2232368 |
ClinGen | rs2232368 |
ebi | rs2232368 |
HLI | rs2232368 |
Exac | rs2232368 |
Gnomad | rs2232368 |
Varsome | rs2232368 |
LitVar | rs2232368 |
Map | rs2232368 |
PheGenI | rs2232368 |
Biobank | rs2232368 |
1000 genomes | rs2232368 |
hgdp | rs2232368 |
ensembl | rs2232368 |
geneview | rs2232368 |
scholar | rs2232368 |
rs2232368 | |
pharmgkb | rs2232368 |
gwascentral | rs2232368 |
openSNP | rs2232368 |
23andMe | rs2232368 |
SNPshot | rs2232368 |
SNPdbe | rs2232368 |
MSV3d | rs2232368 |
GWAS Ctlg | rs2232368 |
GMAF | 0.01632 |
Max Magnitude | 0 |
[PMID 21481380] Analysis of FOXP3 polymorphisms in infertile women with and without endometriosis
[PMID 29476189] The synergic effects of CTLA-4/Foxp3-related genotypes and chromosomal aberrations on the risk of recurrent spontaneous abortion among a Chinese Han population.