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rs12216125

From SNPedia

Orientationplus
Stabilizedplus
Make rs12216125(C;C)
Make rs12216125(C;T)
Make rs12216125(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position25997230
GeneLOC100996311
is asnp
is mentioned by
dbSNPrs12216125
ebirs12216125
HLIrs12216125
Exacrs12216125
Varsomers12216125
Maprs12216125
PheGenIrs12216125
hapmaprs12216125
1000 genomesrs12216125
hgdprs12216125
ensemblrs12216125
gopubmedrs12216125
geneviewrs12216125
scholarrs12216125
googlers12216125
pharmgkbrs12216125
gwascentralrs12216125
openSNPrs12216125
23andMers12216125
23andMe allrs12216125
SNP Nexus

SNPshotrs12216125
SNPdbers12216125
MSV3drs12216125
GWAS Ctlgrs12216125
GMAF0.1869
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000004
Odds Ratio NR NR



GET Evidence
rs12216125
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary