rs2298668
From SNPedia
| Merged into | rs2229437 |
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs2298668(A;C) |
| Make rs2298668(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 82853252 |
| Gene | PRCP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2298668 |
| dbSNP (classic) | rs2298668 |
| ClinGen | rs2298668 |
| ebi | rs2298668 |
| HLI | rs2298668 |
| Exac | rs2298668 |
| Gnomad | rs2298668 |
| Varsome | rs2298668 |
| LitVar | rs2298668 |
| Map | rs2298668 |
| PheGenI | rs2298668 |
| Biobank | rs2298668 |
| 1000 genomes | rs2298668 |
| hgdp | rs2298668 |
| ensembl | rs2298668 |
| geneview | rs2298668 |
| scholar | rs2298668 |
| rs2298668 | |
| pharmgkb | rs2298668 |
| gwascentral | rs2298668 |
| openSNP | rs2298668 |
| 23andMe | rs2298668 |
| SNPshot | rs2298668 |
| SNPdbe | rs2298668 |
| MSV3d | rs2298668 |
| GWAS Ctlg | rs2298668 |
| Status | Merged into rs2229437 |
| GMAF | 0.1383 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
Women with the snp has been linked to significant risk of a premature birth [PMID 16681991]
These press releases explain it more simply
The risky variation is 3x more common in women of african descent.
- rs2298668 Prolylcarboxypepdiase E112D (rs2298668)D allele alone and jointly with chronic hypertension were associated with a significantly increased risk of preeclampsia
[PMID 16642433
] Polymorphism in maternal LRP8 gene is associated with fetal growth.
