RHOH, ras homolog family member H, 399

N. diseases: 42; N. variants: 1
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs148332376
rs148332376
Entrez Id: 399
Gene Symbol: RHOH
RHOH
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		T 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019