TOMM40 c.644-3240T>A

Variant ID: 19-45400747-T-A

NM_001128917.1(TOMM40):c.644-3240T>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Pharmacogenomics polygenic risk score for drug response prediction using PRS-PGx methods.

Nature Communications
Zhai, Song S; Zhang, Hong H; Mehrotra, Devan V DV; Shen, Judong J
Publication Date: 2022-09-08

Variant appearance in text: rs61679753
PubMed Link: 36075892
Variant Present in the following documents:
  • 41467_2022_32407_MOESM1_ESM.pdf
View BVdb publication page



The flashfm approach for fine-mapping multiple quantitative traits.

Nature Communications
Hernández, N N; Soenksen, J J; Newcombe, P P; Sandhu, M M; Barroso, I I; Wallace, C C; Asimit, J L JL
Publication Date: 2021-10-22

Variant appearance in text: rs61679753
PubMed Link: 34686674
Variant Present in the following documents:
  • Main text
  • 41467_2021_Article_26364.pdf
View BVdb publication page



Genetics of 35 blood and urine biomarkers in the UK Biobank.

Nature Genetics
Sinnott-Armstrong, Nasa N; Tanigawa, Yosuke Y; Amar, David D; Mars, Nina N; Benner, Christian C; Aguirre, Matthew M; Venkataraman, Guhan Ram GR; Wainberg, Michael M; Ollila, Hanna M HM; Kiiskinen, Tuomo T; Havulinna, Aki S AS; Pirruccello, James P JP; Qian, Junyang J; Shcherbina, Anna A; , ; Rodriguez, Fatima F; Assimes, Themistocles L TL; Agarwala, Vineeta V; Tibshirani, Robert R; Hastie, Trevor T; Ripatti, Samuli S; Pritchard, Jonathan K JK; Daly, Mark J MJ; Rivas, Manuel A MA
Publication Date: 2021-02

Variant appearance in text: TOMM40: 644-3240T>A; rs61679753
PubMed Link: 33462484
Variant Present in the following documents:
  • NIHMS1651539-supplement-2.xlsx, sheet 21
View BVdb publication page



PheGWAS: a new dimension to visualize GWAS across multiple phenotypes.

Bioinformatics (Oxford, England)
George, Gittu G; Gan, Sushrima S; Huang, Yu Y; Appleby, Philip P; Nar, A S AS; Venkatesan, Radha R; Mohan, Viswanathan V; Palmer, Colin N A CNA; Doney, Alex S F ASF
Publication Date: 2020-04-15

Variant appearance in text: rs61679753
PubMed Link: 31860083
Variant Present in the following documents:
  • Main text
  • btz944.pdf
View BVdb publication page



Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies.

American Journal Of Human Genetics
Benner, Christian C; Havulinna, Aki S AS; Järvelin, Marjo-Riitta MR; Salomaa, Veikko V; Ripatti, Samuli S; Pirinen, Matti M
Publication Date: 2017-10-05

Variant appearance in text: rs61679753
PubMed Link: 28942963
Variant Present in the following documents:
  • Main text
View BVdb publication page



Replication and fine-mapping of genetic predictors of lipid traits in African-Americans.

Journal Of Human Genetics
Feng, QiPing Q; Wei, Wei-Qi WQ; Levinson, Rebecca T RT; Mosley, Jonathan D JD; Stein, C Michael CM
Publication Date: 2017-10

Variant appearance in text: rs61679753
PubMed Link: 28539666
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study.

Circulation. Cardiovascular Genetics
Carty, Cara L CL; Bhattacharjee, Samsiddhi S; Haessler, Jeff J; Cheng, Iona I; Hindorff, Lucia A LA; Aroda, Vanita V; Carlson, Christopher S CS; Hsu, Chun-Nan CN; Wilkens, Lynne L; Liu, Simin S; Selvin, Elizabeth E; Jackson, Rebecca R; North, Kari E KE; Peters, Ulrike U; Pankow, James S JS; Chatterjee, Nilanjan N; Kooperberg, Charles C
Publication Date: 2014-08

Variant appearance in text: rs61679753
PubMed Link: 25023634
Variant Present in the following documents:
  • Main text
View BVdb publication page