Variant ID: 11-116732512-G-T


This variant was identified in 3 publications


Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.

Y Yamada, J Sakuma, I Takeuchi, Y Yasukochi, K Kato, M Oguri, T Fujimaki, H Horibe, M Muramatsu, M Sawabe, Y Fujiwara, Y Taniguchi, S Obuchi, H Kawai, S Shinkai, S Mori, T Arai, M Tanaka
Publication Date: 2017-06-13

Variant appearance in text: rs2075292
PMID: 28473662
View BVdb publication page

Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study.

Cardiovascular Diabetology
CM Povel, JM Boer, NC Onland-Moret, ME Dollé, EJ Feskens, YT van der Schouw
Publication Date: 2012-10-29

Variant appearance in text: rs2075292
PMID: 23101478
View BVdb publication page

Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology
OA Panagiotou, E Evangelou, JP Ioannidis
Publication Date: 2010-10-15

Variant appearance in text: rs2075292
PMID: 20876667
View BVdb publication page

Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000292055.4 c.1997+45C>A - intron_variant - 17/23
ENST00000375288.1 c.292+45C>A - intron_variant - 17/22
ENST00000375300.1 c.2171+45C>A - intron_variant - 17/23
ENST00000415541.1 c.*1695+45C>A - intron_variant,NMD_transcript_variant - 18/24
ENST00000434315.2 c.1694+45C>A - intron_variant - 18/24
ENST00000445177.1 c.2295+45C>A - intron_variant - 18/24
ENST00000446921.2 c.2171+45C>A - intron_variant - 17/23
ENST00000465421.1 n.1613+45C>A - intron_variant,non_coding_transcript_variant - 3/9
ENST00000488337.1 n.474+45C>A - intron_variant,non_coding_transcript_variant - 4/9
ENST00000542607.1 c.1997+45C>A - intron_variant - 17/23
NM_001281748.3 c.1694+45C>A - intron_variant - 18/24
NM_001281749.3 c.2171+45C>A - intron_variant - 17/23
NM_001366686.2 c.2315+45C>A - intron_variant - 18/24
NM_025164.6 c.2171+45C>A - intron_variant - 17/23