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CYP2C9 c.169-1078C>T
Variant ID: 10-96700537-C-T
NM_000771.3(
CYP2C9
):c.169-1078C>T
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: rs2253635
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Polymorphisms in CYP2C9 are associated with response to indomethacin among neonates with patent ductus arteriosus.
Pediatric Research
Smith, Caitlin J CJ; Ryckman, Kelli K KK; Bahr, Timothy M TM; Dagle, John M JM
Publication Date: 2017-11
Variant appearance in text: rs2253635
PubMed Link:
28609430
Variant Present in the following documents:
Main text
View BVdb publication page
Genetic markers in the EET metabolic pathway are associated with outcomes in patients with aneurysmal subarachnoid hemorrhage.
Journal Of Cerebral Blood Flow And Metabolism : Official Journal Of The International Society Of Cerebral Blood Flow And Metabolism
Donnelly, Mark K MK; Conley, Yvette P YP; Crago, Elizabeth A EA; Ren, Dianxu D; Sherwood, Paula R PR; Balzer, Jeffery R JR; Poloyac, Samuel M SM
Publication Date: 2015-02
Variant appearance in text: rs2253635
PubMed Link:
25388680
Variant Present in the following documents:
Main text
View BVdb publication page