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: rs3087869

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

SLC44A2 single nucleotide polymorphisms, isoforms, and expression: Association with severity of Meniere's disease?

Genomics

Nair, Thankam S TS; Kommareddi, Pavan K PK; Galano, Maria M MM; Miller, Danielle M DM; Kakaraparthi, Bala Naveen BN; Telian, Steven A SA; Arts, H Alex HA; El-Kashlan, Hussam H; Kilijanczyk, Alyse A; Lassig, Amy Anne D AA; Graham, Martin P MP; Fisher, Susan G SG; Stoll, Stefan W SW; Nair, Rajan P RP; Elder, James T JT; Carey, Thomas E TE

Publication Date: 2016-12

Variant appearance in text: rs3087869

PubMed Link: 27829169

Variant Present in the following documents:

• Main text

View BVdb publication page