VLDLR c.*551T>C

Variant ID: 9-2654419-T-C

NM_003383.3(VLDLR):c.*551T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs8210
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Monozygotic twins reveal germline contribution to allelic expression differences.

American Journal Of Human Genetics
Cheung, Vivian G VG; Bruzel, Alan A; Burdick, Joshua T JT; Morley, Michael M; Devlin, James L JL; Spielman, Richard S RS
Publication Date: 2008-06

Variant appearance in text: rs8210
PubMed Link: 18513681
Variant Present in the following documents:
  • Main text
View BVdb publication page