CSTF1 c.-33+390G>A

Variant ID: 20-54968159-G-A

NM_001324.3(CSTF1):c.-33+390G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs6064387
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth.

Reproductive Sciences (Thousand Oaks, Calif.)
Haas, David M DM; Lai, Dongbing D; Sharma, Sunita S; Then, Jenny J; Kho, Alvin A; Flockhart, David A DA; Tantisira, Kelan K; Foroud, Tatiana T
Publication Date: 2016-05

Variant appearance in text: rs6064387
PubMed Link: 26507871
Variant Present in the following documents:
  • Main text
View BVdb publication page