SLC22A1 c.1598+393G>C

Variant ID: 6-160577499-G-C

NM_003057.2(SLC22A1):c.1598+393G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Intronic Variants in OCT1 are Associated with All-Cause and Cardiovascular Mortality in Metformin Users with Type 2 Diabetes.

Diabetes, Metabolic Syndrome And Obesity : Targets And Therapy
Schweighofer, Natascha N; Genser, Bernd B; Maerz, Winfried W; Kleber, Marcus E ME; Trummer, Olivia O; Pieber, Thomas R TR; Obermayer-Pietsch, Barbara B
Publication Date: 2020

Variant appearance in text: rs3818678
PubMed Link: 32606866
Variant Present in the following documents:
  • Main text
  • dmso-13-2069.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: rs3818678
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page