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Pregnancy

From SNPedia


Pregnancy is the period from conception to birth, the state of carrying a developing embryo or fetus, or several embryos, within the female body.

Among medical conditions related to pregnancy are pre-eclampsia, premature birth, recurrent miscarriage and Intrahepatic cholestasis of pregnancy.

Some relevant SNPs[edit]

Based on scientific publications e.g. these SNPs seem to have relevance to pregnancy.

rs699

rs4762

rs5186

rs5219

rs5443

rs6025

rs4762

rs222581

rs560887

rs879293

rs975369

rs1248993

rs1387153

rs1556832

rs1799963

rs1799983

rs1799884

rs1801278

rs1982073

rs2273697

rs2287622

rs2298668

rs2839440

rs3740066

rs4402960

rs4815879

rs4841132

rs4696480 in fetal DNA

rs4746822

rs4986791

rs5743708 in fetal DNA

rs6563695

rs7028939

rs7322722

rs7754840

rs7903146

rs8187710

rs9976946

rs10509305

rs10830963

rs10883969

rs10989019

rs11600901

rs11617740

rs12255372

rs12641856

rs17222723

rs17121510 in fetal DNA

rs17412740

rs17636747

rs17787940

rs28360974

rs137852769

Gestational diabetes publications[edit]

[PMID 23690305OA-icon.png] Genetic variants and the risk of gestational diabetes mellitus: a systematic review.

[PMID 22233651OA-icon.png] 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 18984664OA-icon.png] Common type 2 diabetes risk gene variants associate with gestational diabetes.

Intrahepatic cholestasis of pregnancy publications[edit]

[PMID 18987030] Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy.

[PMID 17997497OA-icon.png] Association of the multidrug-resistance-associated protein gene (ABCC2) variants with intrahepatic cholestasis of pregnancy.

Pre-eclampsia publications[edit]

[PMID 23976997OA-icon.png] The common variant rs11646213 is associated with preeclampsia in Han Chinese women.

[PMID 23551011OA-icon.png] 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[edit]

[PMID 25599974OA-icon.png] A genome-wide association study of early spontaneous preterm delivery.

[PMID 25264875OA-icon.png] Pathway analysis of genetic factors associated with spontaneous preterm birth and pre-labor preterm rupture of membranes.

[PMID 23613933OA-icon.png] X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study.

[PMID 23445776OA-icon.png] Genome-wide association studies in preterm birth: implications for the practicing obstetrician-gynaecologist.

[PMID 23227263OA-icon.png] A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers.

[PMID 18818748OA-icon.png] Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variants.

[PMID 18787196OA-icon.png] Segment-specific genetic effects on carotid intima-media thickness: the Northern Manhattan study.

[PMID 17667860OA-icon.png] Toll-like receptor 2 polymorphism is associated with preterm birth.

[PMID 16938879OA-icon.png] A functional SNP in the promoter of the SERPINH1 gene increases risk of preterm premature rupture of membranes in African Americans.

Recurrent miscarriage publications[edit]

[PMID 22457663OA-icon.png] Genetics of recurrent miscarriage: challenges, current knowledge, future directions.

[PMID 21257601OA-icon.png] A genome-wide scan in affected sibling pairs with idiopathic recurrent miscarriage suggests genetic linkage.

[PMID 17997497OA-icon.png] A study of forty-seven single nucleotide polymorphisms among recurrent miscarriage using classification and regression tree analysis.

Links[edit]

In Wikipedia: Pregnancy

In Genetics Home Reference: Preeclampsia