Have questions? Visit https://www.reddit.com/r/SNPedia

rs1020064

From SNPedia

Orientationplus
Stabilizedplus
Make rs1020064(G;G)
Make rs1020064(G;T)
Make rs1020064(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position105281283
GeneTGFBRAP1
is asnp
is mentioned by
dbSNPrs1020064
ebirs1020064
HLIrs1020064
Exacrs1020064
Varsomers1020064
Maprs1020064
PheGenIrs1020064
hapmaprs1020064
1000 genomesrs1020064
hgdprs1020064
ensemblrs1020064
gopubmedrs1020064
geneviewrs1020064
scholarrs1020064
googlers1020064
pharmgkbrs1020064
gwascentralrs1020064
openSNPrs1020064
23andMers1020064
23andMe allrs1020064
SNP Nexus

SNPshotrs1020064
SNPdbers1020064
MSV3drs1020064
GWAS Ctlgrs1020064
GMAF0.1951
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19754311]
Trait AIDS
Title Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).
Risk Allele G
P-val 0.000007
Odds Ratio 2.94 [1.75-5.00]


[PMID 21221856OA-icon.png] The search for host genetic factors of HIV/AIDS pathogenesis in the post-genome era: progress to date and new avenues for discovery.


GET Evidence
rs1020064
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.804688
summary