EGFR c.88+41149A>T

Variant ID: 7-55128207-A-T

NM_005228.3(EGFR):c.88+41149A>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs729969
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Database of genetic studies of bipolar disorder.

Psychiatric Genetics
Piletz, John E JE; Zhang, Xiaotong X; Ranade, Rajdeep R; Liu, Chunyu C
Publication Date: 2011-04

Variant appearance in text: rs729969
PubMed Link: 21085053
Variant Present in the following documents:
  • Main text
View BVdb publication page



Whole-genome association study of bipolar disorder.

Molecular Psychiatry
Sklar, P P; Smoller, J W JW; Fan, J J; Ferreira, M A R MA; Perlis, R H RH; Chambert, K K; Nimgaonkar, V L VL; McQueen, M B MB; Faraone, S V SV; Kirby, A A; de Bakker, P I W PI; Ogdie, M N MN; Thase, M E ME; Sachs, G S GS; Todd-Brown, K K; Gabriel, S B SB; Sougnez, C C; Gates, C C; Blumenstiel, B B; Defelice, M M; Ardlie, K G KG; Franklin, J J; Muir, W J WJ; McGhee, K A KA; MacIntyre, D J DJ; McLean, A A; VanBeck, M M; McQuillin, A A; Bass, N J NJ; Robinson, M M; Lawrence, J J; Anjorin, A A; Curtis, D D; Scolnick, E M EM; Daly, M J MJ; Blackwood, D H DH; Gurling, H M HM; Purcell, S M SM
Publication Date: 2008-06

Variant appearance in text: rs729969
PubMed Link: 18317468
Variant Present in the following documents:
  • Main text
View BVdb publication page