MASP1 c.5+2718G>A

Variant ID: 3-187006698-C-T

NM_139125.3(MASP1):c.5+2718G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Adding MASP1 to the lectin pathway-Leprosy association puzzle: Hints from gene polymorphisms and protein levels.

Plos Neglected Tropical Diseases
Weinschutz Mendes, Hellen H; Boldt, Angelica Beate Winter ABW; von Rosen Seeling Stahlke, Ewalda E; Jensenius, Jens Christian JC; Thiel, Steffen S; Messias-Reason, Iara J Taborda IJT
Publication Date: 2020-04

Variant appearance in text: MASP: 5+2718G>A; rs7609662
PubMed Link: 32240160
Variant Present in the following documents:
  • Main text
  • pntd.0007534.pdf
View BVdb publication page



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: rs7609662
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page