Pregnancy is the period from conception to birth, the state of carrying a developing embryo or fetus, or several embryos, within the female body.
Based on scientific publications e.g. these SNPs seem to have relevance to pregnancy.
rs4696480 in fetal DNA
rs5743708 in fetal DNA
rs17121510 in fetal DNA
Gestational diabetes publications
[PMID 23690305] Genetic variants and the risk of gestational diabetes mellitus: a systematic review.
[PMID 22233651] A genome-wide association study of gestational diabetes mellitus in Korean women.
[PMID 19002430] Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population.
[PMID 18984664] Common type 2 diabetes risk gene variants associate with gestational diabetes.
Intrahepatic cholestasis of pregnancy publications
[PMID 18987030] Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy.
[PMID 17997497] Association of the multidrug-resistance-associated protein gene (ABCC2) variants with intrahepatic cholestasis of pregnancy.
[PMID 23551011] Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.
[PMID 22432041] Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.
[PMID 15806103] Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family.
Premature birth publications
[PMID 25599974] A genome-wide association study of early spontaneous preterm delivery.
[PMID 25264875] Pathway analysis of genetic factors associated with spontaneous preterm birth and pre-labor preterm rupture of membranes.
[PMID 23613933] X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study.
[PMID 23445776] Genome-wide association studies in preterm birth: implications for the practicing obstetrician-gynaecologist.
[PMID 23227263] A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers.
[PMID 18818748] Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variants.
[PMID 18787196] Segment-specific genetic effects on carotid intima-media thickness: the Northern Manhattan study.
[PMID 17667860] Toll-like receptor 2 polymorphism is associated with preterm birth.
[PMID 16938879] A functional SNP in the promoter of the SERPINH1 gene increases risk of preterm premature rupture of membranes in African Americans.
Recurrent miscarriage publications
[PMID 22457663] Genetics of recurrent miscarriage: challenges, current knowledge, future directions.
[PMID 21257601] A genome-wide scan in affected sibling pairs with idiopathic recurrent miscarriage suggests genetic linkage.
[PMID 17997497] A study of forty-seven single nucleotide polymorphisms among recurrent miscarriage using classification and regression tree analysis.
In Wikipedia: Pregnancy
In Genetics Home Reference: Preeclampsia