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rs4516970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4516970(A;A)
Make rs4516970(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position159716655
is asnp
is mentioned by
dbSNPrs4516970
ebirs4516970
HLIrs4516970
Exacrs4516970
Varsomers4516970
Maprs4516970
PheGenIrs4516970
hapmaprs4516970
1000 genomesrs4516970
hgdprs4516970
ensemblrs4516970
gopubmedrs4516970
geneviewrs4516970
scholarrs4516970
googlers4516970
pharmgkbrs4516970
gwascentralrs4516970
openSNPrs4516970
23andMers4516970
23andMe allrs4516970
SNP Nexus

SNPshotrs4516970
SNPdbers4516970
MSV3drs4516970
GWAS Ctlgrs4516970
GMAF0.04454
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 0.000001
Odds Ratio NR NR



GET Evidence
rs4516970
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary