rs1250248
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1250248(A;A) |
Make rs1250248(A;G) |
Make rs1250248(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 215422370 |
Gene | FN1 |
is a | snp |
is | mentioned by |
dbSNP | rs1250248 |
dbSNP (classic) | rs1250248 |
ClinGen | rs1250248 |
ebi | rs1250248 |
HLI | rs1250248 |
Exac | rs1250248 |
Gnomad | rs1250248 |
Varsome | rs1250248 |
LitVar | rs1250248 |
Map | rs1250248 |
PheGenI | rs1250248 |
Biobank | rs1250248 |
1000 genomes | rs1250248 |
hgdp | rs1250248 |
ensembl | rs1250248 |
geneview | rs1250248 |
scholar | rs1250248 |
rs1250248 | |
pharmgkb | rs1250248 |
gwascentral | rs1250248 |
openSNP | rs1250248 |
23andMe | rs1250248 |
SNPshot | rs1250248 |
SNPdbe | rs1250248 |
MSV3d | rs1250248 |
GWAS Ctlg | rs1250248 |
GMAF | 0.1607 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23142796] An Italian association study and meta-analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first identified susceptibility loci for endometriosis
[PMID 23315067] Replication of endometriosis-associated single-nucleotide polymorphisms from genome-wide association studies in a Caucasian population.
[PMID 31115525] Role of FN1 and GREB1 gene polymorphisms in endometriosis.
[PMID 33113402] Systematic review of genome-wide association studies on susceptibility to endometriosis.