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rs17027625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17027625(C;C)
Make rs17027625(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position31404088
GeneTHRAP3P1
is asnp
is mentioned by
dbSNPrs17027625
dbSNP (classic)rs17027625
ClinGenrs17027625
ebirs17027625
HLIrs17027625
Exacrs17027625
Gnomadrs17027625
Varsomers17027625
LitVarrs17027625
Maprs17027625
PheGenIrs17027625
Biobankrs17027625
1000 genomesrs17027625
hgdprs17027625
ensemblrs17027625
geneviewrs17027625
scholarrs17027625
googlers17027625
pharmgkbrs17027625
gwascentralrs17027625
openSNPrs17027625
23andMers17027625
SNPshotrs17027625
SNPdbers17027625
MSV3drs17027625
GWAS Ctlgrs17027625
GMAF0.03627
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20041166OA-icon.png]
Trait HIV-1 control
Title Common Genetic Variation and the Control of HIV-1 in Human
Risk Allele
P-val 0.000004
Odds Ratio NR NR


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