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rs1556032

From SNPedia

Orientationplus
Stabilizedplus
Make rs1556032(C;C)
Make rs1556032(C;T)
Make rs1556032(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position14446003
is asnp
is mentioned by
dbSNPrs1556032
ebirs1556032
HLIrs1556032
Exacrs1556032
Varsomers1556032
Maprs1556032
PheGenIrs1556032
hapmaprs1556032
1000 genomesrs1556032
hgdprs1556032
ensemblrs1556032
gopubmedrs1556032
geneviewrs1556032
scholarrs1556032
googlers1556032
pharmgkbrs1556032
gwascentralrs1556032
openSNPrs1556032
23andMers1556032
23andMe allrs1556032
SNP Nexus

SNPshotrs1556032
SNPdbers1556032
MSV3drs1556032
GWAS Ctlgrs1556032
GMAF0.4187
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 0.000009
Odds Ratio 2.05 [1.48-2.84]


GET Evidence
rs1556032
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary