rs7579169
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7579169(C;C) |
Make rs7579169(C;T) |
Make rs7579169(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 120360548 |
is a | snp |
is | mentioned by |
dbSNP | rs7579169 |
dbSNP (classic) | rs7579169 |
ClinGen | rs7579169 |
ebi | rs7579169 |
HLI | rs7579169 |
Exac | rs7579169 |
Gnomad | rs7579169 |
Varsome | rs7579169 |
LitVar | rs7579169 |
Map | rs7579169 |
PheGenI | rs7579169 |
Biobank | rs7579169 |
1000 genomes | rs7579169 |
hgdp | rs7579169 |
ensembl | rs7579169 |
geneview | rs7579169 |
scholar | rs7579169 |
rs7579169 | |
pharmgkb | rs7579169 |
gwascentral | rs7579169 |
openSNP | rs7579169 |
23andMe | rs7579169 |
SNPshot | rs7579169 |
SNPdbe | rs7579169 |
MSV3d | rs7579169 |
GWAS Ctlg | rs7579169 |
GMAF | 0.2879 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22432041] Genome-Wide Association Scan Identifies a Risk Locus for Preeclampsia on 2q14, Near the Inhibin, Beta B Gene
[PMID 26313529] Single nucleotide polymorphisms near the inhibin beta B gene on 2q14 are associated with pre-eclampsia in Han Chinese women
[PMID 26313396] Association of single nucleotide polymorphism rs7579169 with hypertension disorders during pregnancy and perinatal outcome
[PMID 27173354] Common variant rs7579169 is associated with preeclampsia in Han Chinese women.