ABCA1 c.1311+521G>A

Variant ID: 9-107598740-C-T

NM_005502.3(ABCA1):c.1311+521G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Model of genetic and environmental factors associated with type 2 diabetes mellitus in a Chinese Han population.

Bmc Public Health
Li, Zheng Z; Ye, Cheng-Yin CY; Zhao, Tian-Yu TY; Yang, Lei L
Publication Date: 2020-06-29

Variant appearance in text: rs2065412
PubMed Link: 32600448
Variant Present in the following documents:
  • Main text
  • 12889_2020_Article_9130.pdf
View BVdb publication page



Progress in genome-wide association studies of schizophrenia in Han Chinese populations.

Npj Schizophrenia
Yue, Weihua W; Yu, Xin X; Zhang, Dai D
Publication Date: 2017-08-10

Variant appearance in text: rs2065412
PubMed Link: 28798405
Variant Present in the following documents:
  • Main text
  • 41537_2017_Article_29.pdf
View BVdb publication page



3'UTR Polymorphism in ACSL1 Gene Correlates with Expression Levels and Poor Clinical Outcome in Colon Cancer Patients.

Plos One
Vargas, Teodoro T; Moreno-Rubio, Juan J; Herranz, Jesús J; Cejas, Paloma P; Molina, Susana S; Mendiola, Marta M; Burgos, Emilio E; Custodio, Ana B AB; De Miguel, María M; Martín-Hernández, Roberto R; Reglero, Guillermo G; Feliu, Jaime J; Ramírez de Molina, Ana A
Publication Date: 2016

Variant appearance in text: rs2065412
PubMed Link: 27992526
Variant Present in the following documents:
  • Main text
  • pone.0168423.pdf
View BVdb publication page



Evolutionary responses to a constructed niche: ancient Mesoamericans as a model of gene-culture coevolution.

Plos One
Hünemeier, Tábita T; Amorim, Carlos Eduardo Guerra CE; Azevedo, Soledad S; Contini, Veronica V; Acuña-Alonzo, Víctor V; Rothhammer, Francisco F; Dugoujon, Jean-Michel JM; Mazières, Stephane S; Barrantes, Ramiro R; Villarreal-Molina, María Teresa MT; Paixão-Côrtes, Vanessa Rodrigues VR; Salzano, Francisco M FM; Canizales-Quinteros, Samuel S; Ruiz-Linares, Andres A; Bortolini, Maria Cátira MC
Publication Date: 2012

Variant appearance in text: rs2065412
PubMed Link: 22768049
Variant Present in the following documents:
  • Main text
View BVdb publication page



Chromosome 3 anomalies investigated by genome wide SNP analysis of benign, low malignant potential and low grade ovarian serous tumours.

Plos One
Birch, Ashley H AH; Arcand, Suzanna L SL; Oros, Kathleen K KK; Rahimi, Kurosh K; Watters, A Kevin AK; Provencher, Diane D; Greenwood, Celia M CM; Mes-Masson, Anne-Marie AM; Tonin, Patricia N PN
Publication Date: 2011

Variant appearance in text: rs2065412
PubMed Link: 22163003
Variant Present in the following documents:
  • Main text
  • pone.0028250.pdf
View BVdb publication page



Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk.

Human Molecular Genetics
Reynolds, Chandra A CA; Hong, Mun-Gwan MG; Eriksson, Ulrika K UK; Blennow, Kaj K; Wiklund, Fredrik F; Johansson, Boo B; Malmberg, Bo B; Berg, Stig S; Alexeyenko, Andrey A; Grönberg, Henrik H; Gatz, Margaret M; Pedersen, Nancy L NL; Prince, Jonathan A JA
Publication Date: 2010-05-15

Variant appearance in text: rs2065412
PubMed Link: 20167577
Variant Present in the following documents:
  • Main text
View BVdb publication page



A survey of ABCA1 sequence variation confirms association with dementia.

Human Mutation
Reynolds, Chandra A CA; Hong, Mun-Gwan MG; Eriksson, Ulrika K UK; Blennow, Kaj K; Bennet, Anna M AM; Johansson, Boo B; Malmberg, Bo B; Berg, Stig S; Wiklund, Fredrik F; Gatz, Margaret M; Pedersen, Nancy L NL; Prince, Jonathan A JA
Publication Date: 2009-09

Variant appearance in text: rs2065412
PubMed Link: 19606474
Variant Present in the following documents:
  • Main text
View BVdb publication page