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rs1522232

From SNPedia

Orientationplus
Stabilizedplus
Make rs1522232(C;C)
Make rs1522232(C;T)
Make rs1522232(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position24241438
GeneRP11-778H2.1, SOX5
is asnp
is mentioned by
dbSNPrs1522232
ebirs1522232
HLIrs1522232
Exacrs1522232
Varsomers1522232
Maprs1522232
PheGenIrs1522232
hapmaprs1522232
1000 genomesrs1522232
hgdprs1522232
ensemblrs1522232
gopubmedrs1522232
geneviewrs1522232
scholarrs1522232
googlers1522232
pharmgkbrs1522232
gwascentralrs1522232
openSNPrs1522232
23andMers1522232
23andMe allrs1522232
SNP Nexus

SNPshotrs1522232
SNPdbers1522232
MSV3drs1522232
GWAS Ctlgrs1522232
GMAF0.3912
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 0.000002
Odds Ratio 2.22 [1.59-3.13]


[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
rs1522232
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.414062
summary