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rs1000916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1000916(A;G)
Make rs1000916(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position31091689
GeneGALNT14
is asnp
is mentioned by
dbSNPrs1000916
ebirs1000916
HLIrs1000916
Exacrs1000916
Varsomers1000916
Maprs1000916
PheGenIrs1000916
hapmaprs1000916
1000 genomesrs1000916
hgdprs1000916
ensemblrs1000916
gopubmedrs1000916
geneviewrs1000916
scholarrs1000916
googlers1000916
pharmgkbrs1000916
gwascentralrs1000916
openSNPrs1000916
23andMers1000916
23andMe allrs1000916
SNP Nexus

SNPshotrs1000916
SNPdbers1000916
MSV3drs1000916
GWAS Ctlgrs1000916
GMAF0.05601
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22174851OA-icon.png]
Trait
Title Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.
Risk Allele
P-val 0.000009
Odds Ratio None None