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rs2718812

From SNPedia

Orientationminus
Stabilizedminus
Make rs2718812(A;A)
Make rs2718812(A;G)
Make rs2718812(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position133680858
is asnp
is mentioned by
dbSNPrs2718812
ebirs2718812
HLIrs2718812
Exacrs2718812
Varsomers2718812
Maprs2718812
PheGenIrs2718812
hapmaprs2718812
1000 genomesrs2718812
hgdprs2718812
ensemblrs2718812
gopubmedrs2718812
geneviewrs2718812
scholarrs2718812
googlers2718812
pharmgkbrs2718812
gwascentralrs2718812
openSNPrs2718812
23andMers2718812
23andMe allrs2718812
SNP Nexus

SNPshotrs2718812
SNPdbers2718812
MSV3drs2718812
GWAS Ctlgrs2718812
GMAF0.4807
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19084217OA-icon.png]
Trait Serum markers of iron status
Title Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels
Risk Allele
P-val 0.000001
Odds Ratio NR NR



GET Evidence
rs2718812
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.578125
summary