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rs17154929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17154929(C;T)
Make rs17154929(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position44029227
is asnp
is mentioned by
dbSNPrs17154929
ebirs17154929
HLIrs17154929
Exacrs17154929
Varsomers17154929
Maprs17154929
PheGenIrs17154929
hapmaprs17154929
1000 genomesrs17154929
hgdprs17154929
ensemblrs17154929
gopubmedrs17154929
geneviewrs17154929
scholarrs17154929
googlers17154929
pharmgkbrs17154929
gwascentralrs17154929
openSNPrs17154929
23andMers17154929
23andMe allrs17154929
SNP Nexus

SNPshotrs17154929
SNPdbers17154929
MSV3drs17154929
GWAS Ctlgrs17154929
GMAF0.04867
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22628157OA-icon.png]
Trait
Title Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.
Risk Allele T
P-val 1E-7
Odds Ratio None None