ABCC4 c.2535+2222A>T

Variant ID: 13-95765954-T-A

NM_005845.3(ABCC4):c.2535+2222A>T

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.

Molecular Pain
Nishizawa, Daisuke D; Iseki, Masako M; Arita, Hideko H; Hanaoka, Kazuo K; Yajima, Choku C; Kato, Jitsu J; Ogawa, Setsuro S; Hiranuma, Ayako A; Kasai, Shinya S; Hasegawa, Junko J; Hayashida, Masakazu M; Ikeda, Kazutaka K
Publication Date: 2021

Variant appearance in text: rs1678395
PubMed Link: 33685280
Variant Present in the following documents:
  • Main text
  • 10.1177_1744806921999924.pdf
View BVdb publication page


Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.

Molecular Pain
Nishizawa, Daisuke D; Iseki, Masako M; Arita, Hideko H; Hanaoka, Kazuo K; Yajima, Choku C; Kato, Jitsu J; Ogawa, Setsuro S; Hiranuma, Ayako A; Kasai, Shinya S; Hasegawa, Junko J; Hayashida, Masakazu M; Ikeda, Kazutaka K
Publication Date: 2021

Variant appearance in text: rs1678395
PubMed Link: 33685280
Variant Present in the following documents:
  • Main text
  • 10.1177_1744806921999924.pdf
View BVdb publication page


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: rs1678395
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page