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rs4118325

From SNPedia

Orientationplus
Stabilizedplus
Make rs4118325(A;A)
Make rs4118325(A;G)
Make rs4118325(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position107035210
is asnp
is mentioned by
dbSNPrs4118325
ebirs4118325
HLIrs4118325
Exacrs4118325
Varsomers4118325
Maprs4118325
PheGenIrs4118325
hapmaprs4118325
1000 genomesrs4118325
hgdprs4118325
ensemblrs4118325
gopubmedrs4118325
geneviewrs4118325
scholarrs4118325
googlers4118325
pharmgkbrs4118325
gwascentralrs4118325
openSNPrs4118325
23andMers4118325
23andMe allrs4118325
SNP Nexus

SNPshotrs4118325
SNPdbers4118325
MSV3drs4118325
GWAS Ctlgrs4118325
GMAF0.1901
Max Magnitude
? (A;A) (A;G) (G;G) 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 6E-7
Odds Ratio 4.17 [2.17-8.33]


[PMID 20823317OA-icon.png] is-rSNP: a novel technique for in silico regulatory SNP detection.


[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
rs4118325
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary