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: rs7571895

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.

American Journal Of Human Genetics

Franke, Lude L; de Kovel, Carolien G F CG; Aulchenko, Yurii S YS; Trynka, Gosia G; Zhernakova, Alexandra A; Hunt, Karen A KA; Blauw, Hylke M HM; van den Berg, Leonard H LH; Ophoff, Roel R; Deloukas, Panagiotis P; van Heel, David A DA; Wijmenga, Cisca C

Publication Date: 2008-06

Variant appearance in text: rs7571895

PubMed Link: 18519066

Variant Present in the following documents:

• Main text

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