STARD3 c.459G>A ;(p.L153=)

Variant ID: 17-37814687-G-A

NM_006804.3(STARD3):c.459G>A;(p.L153=)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.

Biological Psychiatry
Brazel, David M DM; Jiang, Yu Y; Hughey, Jordan M JM; Turcot, Valérie V; Zhan, Xiaowei X; Gong, Jian J; Batini, Chiara C; Weissenkampen, J Dylan JD; Liu, MengZhen M; , ; , ; Barnes, Daniel R DR; Bertelsen, Sarah S; Chou, Yi-Ling YL; Erzurumluoglu, A Mesut AM; Faul, Jessica D JD; Haessler, Jeff J; Hammerschlag, Anke R AR; Hsu, Chris C; Kapoor, Manav M; Lai, Dongbing D; Le, Nhung N; de Leeuw, Christiaan A CA; Loukola, Anu A; Mangino, Massimo M; Melbourne, Carl A CA; Pistis, Giorgio G; Qaiser, Beenish B; Rohde, Rebecca R; Shao, Yaming Y; Stringham, Heather H; Wetherill, Leah L; Zhao, Wei W; Agrawal, Arpana A; Bierut, Laura L; Chen, Chu C; Eaton, Charles B CB; Goate, Alison A; Haiman, Christopher C; Heath, Andrew A; Iacono, William G WG; Martin, Nicholas G NG; Polderman, Tinca J TJ; Reiner, Alex A; Rice, John J; Schlessinger, David D; Scholte, H Steven HS; Smith, Jennifer A JA; Tardif, Jean-Claude JC; Tindle, Hilary A HA; van der Leij, Andries R AR; Boehnke, Michael M; Chang-Claude, Jenny J; Cucca, Francesco F; David, Sean P SP; Foroud, Tatiana T; Howson, Joanna M M JMM; Kardia, Sharon L R SLR; Kooperberg, Charles C; Laakso, Markku M; Lettre, Guillaume G; Madden, Pamela P; McGue, Matt M; North, Kari K; Posthuma, Danielle D; Spector, Timothy T; Stram, Daniel D; Tobin, Martin D MD; Weir, David R DR; Kaprio, Jaakko J; Abecasis, Gonçalo R GR; Liu, Dajiang J DJ; Vrieze, Scott S
Publication Date: 2019-06-01

Variant appearance in text: rs36015615
PubMed Link: 30679032
Variant Present in the following documents:
  • Main text
View BVdb publication page



The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine.

Genome Medicine
Garofalo, Andrea A; Sholl, Lynette L; Reardon, Brendan B; Taylor-Weiner, Amaro A; Amin-Mansour, Ali A; Miao, Diana D; Liu, David D; Oliver, Nelly N; MacConaill, Laura L; Ducar, Matthew M; Rojas-Rudilla, Vanesa V; Giannakis, Marios M; Ghazani, Arezou A; Gray, Stacy S; Janne, Pasi P; Garber, Judy J; Joffe, Steve S; Lindeman, Neal N; Wagle, Nikhil N; Garraway, Levi A LA; Van Allen, Eliezer M EM
Publication Date: 2016-07-26

Variant appearance in text: rs36015615
PubMed Link: 27460824
Variant Present in the following documents:
  • 13073_2016_333_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.

Nature Genetics
Seddon, Johanna M JM; Yu, Yi Y; Miller, Elizabeth C EC; Reynolds, Robyn R; Tan, Perciliz L PL; Gowrisankar, Sivakumar S; Goldstein, Jacqueline I JI; Triebwasser, Michael M; Anderson, Holly E HE; Zerbib, Jennyfer J; Kavanagh, David D; Souied, Eric E; Katsanis, Nicholas N; Daly, Mark J MJ; Atkinson, John P JP; Raychaudhuri, Soumya S
Publication Date: 2013-11

Variant appearance in text: rs36015615
PubMed Link: 24036952
Variant Present in the following documents:
  • NIHMS512112-supplement-2.xlsx, sheet 2
View BVdb publication page