Annotation Detail

Information

Associated Genes: TNF
Associated Variants: TNF c.-488G>A
TNF c.-488G>A
Associated Disease: Human immunodeficiency virus dementia, susceptibility to
Source Database: ClinVar
Description: NM_000594.3(TNF):c.-488G>A AND Human immunodeficiency virus dementia, susceptibility to
ClinVar Allele ID: 227757
Clinical Significance Description: risk factor
Clinical Significance Last Update: 2006-03-01
Clinical Significance Review Status: no assertion criteria provided
URL: https://www.ncbi.nlm.nih.gov/clinvar/RCV001807638
ClinVar Disease: Human immunodeficiency virus dementia, susceptibility to
Observed Origin Sample: germline
Pubmed: 14718719
Pubmed: 11826025
Pubmed: 11261930
Pubmed: 12485196
Pubmed: 12746914
Pubmed: 9818939
Pubmed: 14681301
Pubmed: 10450718
Pubmed: 11506397
Pubmed: 11896460
Pubmed: 8056188
Pubmed: 16865291
Pubmed: 16418737

Drugs