INSR c.653-27193A>G

Variant ID: 19-7211841-T-C

NM_000208.2(INSR):c.653-27193A>G

This variant was identified in 3 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: rs3745545
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Insulin receptor variants and obesity-related cancers in the Framingham Heart Study.

Cancer Causes & Control : Ccc
Parekh, Niyati N; Guffanti, Guia G; Lin, Yong Y; Ochs-Balcom, Heather M HM; Makarem, Nour N; Hayes, Richard R
Publication Date: 2015-08

Variant appearance in text: rs3745545
PubMed Link: 26077721
Variant Present in the following documents:
  • Main text
View BVdb publication page



The association between polymorphism of INSR and polycystic ovary syndrome: a meta-analysis.

International Journal Of Molecular Sciences
Feng, Chun C; Lv, Ping-Ping PP; Yu, Tian-Tian TT; Jin, Min M; Shen, Jin-Ming JM; Wang, Xue X; Zhou, Feng F; Jiang, Shi-Wen SW
Publication Date: 2015-01-22

Variant appearance in text: rs3745545
PubMed Link: 25622255
Variant Present in the following documents:
  • Main text
  • ijms-16-02403.pdf
View BVdb publication page