SERPINC1 c.1219-856C>T

Variant ID: 1-173874059-G-A

NM_000488.3(SERPINC1):c.1219-856C>T

This variant was identified in 3 publications

View GRCh38 version.




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: rs2227617
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs2227617
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page



Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.

Blood
Ashley-Koch, Allison E AE; Elliott, Laine L; Kail, Melanie E ME; De Castro, Laura M LM; Jonassaint, Jude J; Jackson, Terry L TL; Price, Jennifer J; Ataga, Kenneth I KI; Levesque, Marc C MC; Weinberg, J Brice JB; Orringer, Eugene P EP; Collins, Ann A; Vance, Jeffery M JM; Telen, Marilyn J MJ
Publication Date: 2008-06-15

Variant appearance in text: rs2227617
PubMed Link: 18187665
Variant Present in the following documents:
  • Main text
View BVdb publication page