rs1519761
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1519761(A;A) |
Make rs1519761(A;G) |
Make rs1519761(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 150776690 |
is a | snp |
is | mentioned by |
dbSNP | rs1519761 |
dbSNP (classic) | rs1519761 |
ClinGen | rs1519761 |
ebi | rs1519761 |
HLI | rs1519761 |
Exac | rs1519761 |
Gnomad | rs1519761 |
Varsome | rs1519761 |
LitVar | rs1519761 |
Map | rs1519761 |
PheGenI | rs1519761 |
Biobank | rs1519761 |
1000 genomes | rs1519761 |
hgdp | rs1519761 |
ensembl | rs1519761 |
geneview | rs1519761 |
scholar | rs1519761 |
rs1519761 | |
pharmgkb | rs1519761 |
gwascentral | rs1519761 |
openSNP | rs1519761 |
23andMe | rs1519761 |
SNPshot | rs1519761 |
SNPdbe | rs1519761 |
MSV3d | rs1519761 |
GWAS Ctlg | rs1519761 |
GMAF | 0.4284 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23472165] Genome-wide association study link novel Loci to endometriosis
[PMID 26337243] Independent Replication and Meta-Analysis for Endometriosis Risk Loci
[PMID 30010178] The assessment of GWAS - identified polymorphisms associated with infertility risk in Polish women with endometriosis.