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rs2749097

From SNPedia

Orientationminus
Stabilizedminus
Make rs2749097(C;C)
Make rs2749097(C;G)
Make rs2749097(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position63661797
GenePGM1
is asnp
is mentioned by
dbSNPrs2749097
ebirs2749097
HLIrs2749097
Exacrs2749097
Varsomers2749097
Maprs2749097
PheGenIrs2749097
hapmaprs2749097
1000 genomesrs2749097
hgdprs2749097
ensemblrs2749097
gopubmedrs2749097
geneviewrs2749097
scholarrs2749097
googlers2749097
pharmgkbrs2749097
gwascentralrs2749097
openSNPrs2749097
23andMers2749097
23andMe allrs2749097
SNP Nexus

SNPshotrs2749097
SNPdbers2749097
MSV3drs2749097
GWAS Ctlgrs2749097
GMAF0.2176
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21665994OA-icon.png]
Trait
Title Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.
Risk Allele G
P-val 2E-9
Odds Ratio 0.1200 [0.08-0.16] unit decrease