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rs29880

From SNPedia

Orientationplus
Stabilizedplus
Make rs29880(A;A)
Make rs29880(A;G)
Make rs29880(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position40914882
is asnp
is mentioned by
dbSNPrs29880
ebirs29880
HLIrs29880
Exacrs29880
Varsomers29880
Maprs29880
PheGenIrs29880
hapmaprs29880
1000 genomesrs29880
hgdprs29880
ensemblrs29880
gopubmedrs29880
geneviewrs29880
scholarrs29880
googlers29880
pharmgkbrs29880
gwascentralrs29880
openSNPrs29880
23andMers29880
23andMe allrs29880
SNP Nexus

SNPshotrs29880
SNPdbers29880
MSV3drs29880
GWAS Ctlgrs29880
GMAF0.1501
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 0.000007
Odds Ratio NR NR



GET Evidence
rs29880
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary