SCARB1 c.1128+904G>A

Variant ID: 12-125283766-C-T

NM_005505.4(SCARB1):c.1128+904G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs10773105
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



Plasma lipid levels and risk of primary open angle glaucoma: a genetic study using Mendelian randomization.

Bmc Ophthalmology
Xu, Mengqiao M; Li, Shengguo S; Zhu, Jundong J; Luo, Dawei D; Song, Weitao W; Zhou, Minwen M
Publication Date: 2020-10-02

Variant appearance in text: rs10773105
PubMed Link: 33008364
Variant Present in the following documents:
  • Main text
  • 12886_2020_Article_1661.pdf
View BVdb publication page



Selecting likely causal risk factors from high-throughput experiments using multivariable Mendelian randomization.

Nature Communications
Zuber, Verena V; Colijn, Johanna Maria JM; Klaver, Caroline C; Burgess, Stephen S
Publication Date: 2020-01-07

Variant appearance in text: rs10773105
PubMed Link: 31911605
Variant Present in the following documents:
  • 41467_2019_13870_MOESM1_ESM.pdf
View BVdb publication page



A Mendelian randomization study of the effects of blood lipids on breast cancer risk.

Nature Communications
Nowak, Christoph C; Ärnlöv, Johan J
Publication Date: 2018-09-27

Variant appearance in text: rs10773105
PubMed Link: 30262900
Variant Present in the following documents:
  • 41467_2018_6467_MOESM1_ESM.pdf
View BVdb publication page



Role of Blood Lipids in the Development of Ischemic Stroke and its Subtypes: A Mendelian Randomization Study.

Stroke
Hindy, George G; Engström, Gunnar G; Larsson, Susanna C SC; Traylor, Matthew M; Markus, Hugh S HS; Melander, Olle O; Orho-Melander, Marju M; ,
Publication Date: 2018-04

Variant appearance in text: rs10773105
PubMed Link: 29535274
Variant Present in the following documents:
  • str-49-820-s001.pdf
View BVdb publication page



Association between genetic loci linked to HDL-C levels and Indian patients with CAD: a pilot study.

Heart Asia
Stanley, Ashley A; Ponde, C K CK; Rajani, R M RM; Ashavaid, T F TF
Publication Date: 2017

Variant appearance in text: rs10773105
PubMed Link: 28123455
Variant Present in the following documents:
  • Main text
View BVdb publication page



Single nucleotide polymorphisms in CETP, SLC46A1, SLC19A1, CD36, BCMO1, APOA5, and ABCA1 are significant predictors of plasma HDL in healthy adults.

Lipids In Health And Disease
Clifford, Andrew J AJ; Rincon, Gonzalo G; Owens, Janel E JE; Medrano, Juan F JF; Moshfegh, Alanna J AJ; Baer, David J DJ; Novotny, Janet A JA
Publication Date: 2013-05-08

Variant appearance in text: rs10773105
PubMed Link: 23656756
Variant Present in the following documents:
  • Main text
  • 1476-511X-12-66.pdf
View BVdb publication page