PMS1 c.582+6865G>A

Variant ID: 2-190689771-G-A

NM_000534.4(PMS1):c.582+6865G>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: rs1233284
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



A novel survival multifactor dimensionality reduction method for detecting gene-gene interactions with application to bladder cancer prognosis.

Human Genetics
Gui, Jiang J; Moore, Jason H JH; Kelsey, Karl T KT; Marsit, Carmen J CJ; Karagas, Margaret R MR; Andrew, Angeline S AS
Publication Date: 2011-01

Variant appearance in text: rs1233284
PubMed Link: 20981448
Variant Present in the following documents:
  • Main text
View BVdb publication page