MRPL37 c.646+2014C>T

Variant ID: 1-54673097-C-T

NM_016491.3(MRPL37):c.646+2014C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Risk prediction of recurrent venous thromboembolism: a multiple genetic risk model.

Journal Of Thrombosis And Thrombolysis
Ahmad, Abrar A; Sundquist, Kristina K; Palmér, Karolina K; Svensson, Peter J PJ; Sundquist, Jan J; Memon, Ashfaque A AA
Publication Date: 2019-02

Variant appearance in text: rs10888838
PubMed Link: 30368761
Variant Present in the following documents:
  • Main text
  • 11239_2018_Article_1762.pdf
View BVdb publication page



Genetic variations related to maternal whole blood mitochondrial DNA copy number: a genome-wide and candidate gene study.

The Journal Of Maternal-Fetal & Neonatal Medicine : The Official Journal Of The European Association Of Perinatal Medicine, The Federation Of Asia And Oceania Perinatal Societies, The International Society Of Perinatal Obstetricians
Workalemahu, Tsegaselassie T; Enquobahrie, Daniel A DA; Tadesse, Mahlet G MG; Hevner, Karin K; Gelaye, Bizu B; Sanchez, Sixto E SE; Williams, Michelle A MA
Publication Date: 2017-10

Variant appearance in text: rs10888838
PubMed Link: 27806667
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci.

Plos One
López, Sonia S; Buil, Alfonso A; Souto, Juan Carlos JC; Casademont, Jordi J; Blangero, John J; Martinez-Perez, Angel A; Fontcuberta, Jordi J; Lathrop, Mark M; Almasy, Laura L; Soria, Jose Manuel JM
Publication Date: 2012

Variant appearance in text: rs10888838
PubMed Link: 22916149
Variant Present in the following documents:
  • Main text
  • pone.0042711.pdf
View BVdb publication page