MARC1 c.754-2137A>C

Variant ID: 1-220976257-A-C

NM_022746.3(MARC1):c.754-2137A>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24

Variant appearance in text: rs17008806
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page



Germline mutations in MSR1, ASCC1, and CTHRC1 in patients with Barrett esophagus and esophageal adenocarcinoma.

Jama
Orloff, Mohammed M; Peterson, Charissa C; He, Xin X; Ganapathi, Shireen S; Heald, Brandie B; Yang, Yi-ran YR; Bebek, Gurkan G; Romigh, Todd T; Song, Jee Hoon JH; Wu, Wenjing W; David, Stefan S; Cheng, Yulan Y; Meltzer, Stephen J SJ; Eng, Charis C
Publication Date: 2011-07-27

Variant appearance in text: rs17008806
PubMed Link: 21791690
Variant Present in the following documents:
  • Main text
View BVdb publication page