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SLC22A1 c.839+886C>G
Variant ID: 6-160556043-C-G
NM_003057.2(
SLC22A1
):c.839+886C>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: rs3798172
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Metabolic heritability at birth: implications for chronic disease research.
Human Genetics
Ryckman, Kelli K KK; Smith, Caitlin J CJ; Jelliffe-Pawlowski, Laura L LL; Momany, Allison M AM; Berberich, Stanton L SL; Murray, Jeffrey C JC
Publication Date: 2014-08
Variant appearance in text: rs3798172
PubMed Link:
24850141
Variant Present in the following documents:
Main text
View BVdb publication page
SLC22A1-ABCB1 haplotype profiles predict imatinib pharmacokinetics in Asian patients with chronic myeloid leukemia.
Plos One
Singh, Onkar O; Chan, Jason Yongsheng JY; Lin, Keegan K; Heng, Charles Chuah Thuan CC; Chowbay, Balram B
Publication Date: 2012
Variant appearance in text: rs3798172
PubMed Link:
23272163
Variant Present in the following documents:
Main text
pone.0051771.pdf
View BVdb publication page