Condition: Premature Birth
rs3181382
in
ADCY4
gene and
Premature Birth
PMID 29538362
2018 Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8.
rs867410737
in
ATP5F1D
gene and
Premature Birth
PMID 29478781
2018 Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
rs9927732
in
BANP
gene and
Premature Birth
PMID 29538362
2018 Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8.
rs779027563
in
CNTNAP1
gene and
Premature Birth
PMID 27668699
2017 Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy.
rs11161721
in
COL24A1
gene and
Premature Birth
PMID 28598419
2017 We show that maternal COL24A1 variants have a significant genome-wide interaction with maternal pre-pregnancy overweight/obesity on
PTB
risk, with
rs11161721
(P<sub>G × E</sub>=1.8 × 10<sup>-8</sup>; empirical P<sub>G × E</sub>=1.2 × 10<sup>-8</sup>) as the top hit.
rs201450565
in
EEFSEC
gene and
Premature Birth
PMID 28877031
2017 Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.
rs1559810905
in
IFIH1
gene and
Premature Birth
PMID 30965144
2020 An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1.
rs1034395178
in
LZTR1
gene and
Premature Birth
PMID 29469822
2018 Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants.
rs372271081
in
MICOS10-NBL1;NBL1
gene and
Premature Birth
PMID 30113228
2018 Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants.
rs587777893
in
MTOR
gene and
Premature Birth
PMID 27159400
2016 Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.
rs11466328
in
TGFB1
gene and
Premature Birth
PMID 28877031
2017 Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.