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rs3108919

From SNPedia

Orientationplus
Stabilizedplus
Make rs3108919(C;C)
Make rs3108919(C;T)
Make rs3108919(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position100829318
is asnp
is mentioned by
dbSNPrs3108919
ebirs3108919
HLIrs3108919
Exacrs3108919
Varsomers3108919
Maprs3108919
PheGenIrs3108919
hapmaprs3108919
1000 genomesrs3108919
hgdprs3108919
ensemblrs3108919
gopubmedrs3108919
geneviewrs3108919
scholarrs3108919
googlers3108919
pharmgkbrs3108919
gwascentralrs3108919
openSNPrs3108919
23andMers3108919
23andMe allrs3108919
SNP Nexus

SNPshotrs3108919
SNPdbers3108919
MSV3drs3108919
GWAS Ctlgrs3108919
GMAF0.5
Max Magnitude
? (C;C) (C;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 C
P-val 0.000004
Odds Ratio 2.13 [1.56-2.91]


GET Evidence
rs3108919
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.546875
summary