Variant ID: 1-203108508-T-C

NM_000674.2(ADORA1):c.341+10198T>C

This variant was identified in 6 publications




Publications:


The pharmacogenomics of severe traumatic brain injury.

Pharmacogenomics
SM Adams, YP Conley, AK Wagner, RM Jha, RS Clark, SM Poloyac, PM Kochanek, PE Empey
Publication Date: 2017-10

Variant appearance in text: rs10920573
PubMed Link: 28975867
Variant Present in the following documents:
  • Main text
View BVdb publication page



Detection and interpretation of shared genetic influences on 42 human traits.

Nature Genetics
JK Pickrell, T Berisa, JZ Liu, L Ségurel, JY Tung, DA Hinds
Publication Date: 2016-07

Variant appearance in text: rs10920573
PubMed Link: 27182965
Variant Present in the following documents:
  • NIHMS780506-supplement-6.pdf
View BVdb publication page



Genome-wide association study of metabolic syndrome in koreans.

Genomics & Informatics
SW Jeong, M Chung, SJ Park, SB Cho, KW Hong
Publication Date: 2014-12

Variant appearance in text: rs10920573
PubMed Link: 25705157
Variant Present in the following documents:
  • gni-12-187-s002.pdf
View BVdb publication page



IL-1β associations with posttraumatic epilepsy development: a genetics and biomarker cohort study.

Epilepsia
ML Diamond, AC Ritter, MD Failla, JA Boles, YP Conley, PM Kochanek, AK Wagner
Publication Date: 2014-07

Variant appearance in text: rs10920573
PubMed Link: 24754437
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics and outcomes after traumatic brain injury (TBI): what do we know about pediatric TBI?

Journal Of Pediatric Rehabilitation Medicine
B Kurowski, LJ Martin, SL Wade
Publication Date: 2012

Variant appearance in text: rs10920573
PubMed Link: 23023254
Variant Present in the following documents:
  • Main text
View BVdb publication page



Adenosine A1 receptor gene variants associated with post-traumatic seizures after severe TBI.

Epilepsy Research
AK Wagner, MA Miller, J Scanlon, D Ren, PM Kochanek, YP Conley
Publication Date: 2010-08

Variant appearance in text: rs10920573
PubMed Link: 20609566
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000309502.3 c.341+10198T>C - intron_variant - 5/5
ENST00000337894.4 c.341+10198T>C - intron_variant - 3/3
ENST00000367235.1 c.341+10198T>C - intron_variant - 2/2
ENST00000367236.4 c.341+10198T>C - intron_variant - 2/2
ENST00000464019.1 n.65+9682T>C - intron_variant,non_coding_transcript_variant - 1/1
NM_000674.3 c.341+10198T>C - intron_variant - 3/3
NM_001048230.2 c.341+10198T>C - intron_variant - 2/2
NM_001365065.1 c.-69+10198T>C - intron_variant - 2/2
NM_001365066.1 c.-8+10123T>C - intron_variant - 2/2