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rs1867504

From SNPedia

Orientationplus
Stabilizedplus
Make rs1867504(A;A)
Make rs1867504(A;G)
Make rs1867504(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position133691817
GeneTFP
is asnp
is mentioned by
dbSNPrs1867504
ebirs1867504
HLIrs1867504
Exacrs1867504
Varsomers1867504
Maprs1867504
PheGenIrs1867504
hapmaprs1867504
1000 genomesrs1867504
hgdprs1867504
ensemblrs1867504
gopubmedrs1867504
geneviewrs1867504
scholarrs1867504
googlers1867504
pharmgkbrs1867504
gwascentralrs1867504
openSNPrs1867504
23andMers1867504
23andMe allrs1867504
SNP Nexus

SNPshotrs1867504
SNPdbers1867504
MSV3drs1867504
GWAS Ctlgrs1867504
GMAF0.4187
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 0.000002
Odds Ratio NR NR



GET Evidence
rs1867504
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.601562
summary