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rs1457451

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs1457451(A;A)
Make rs1457451(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position65635244
GeneLOC100131818
is asnp
is mentioned by
dbSNPrs1457451
ebirs1457451
HLIrs1457451
Exacrs1457451
Varsomers1457451
Maprs1457451
PheGenIrs1457451
hapmaprs1457451
1000 genomesrs1457451
hgdprs1457451
ensemblrs1457451
gopubmedrs1457451
geneviewrs1457451
scholarrs1457451
googlers1457451
pharmgkbrs1457451
gwascentralrs1457451
openSNPrs1457451
23andMers1457451
23andMe allrs1457451
SNP Nexus

SNPshotrs1457451
SNPdbers1457451
MSV3drs1457451
GWAS Ctlgrs1457451
GMAF0.1414
Max Magnitude0
? (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 0.000003
Odds Ratio NR NR



GET Evidence
rs1457451
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary