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rs972275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0
Make rs972275(C;C)
Make rs972275(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position127070699
is asnp
is mentioned by
dbSNPrs972275
ebirs972275
HLIrs972275
Exacrs972275
Varsomers972275
Maprs972275
PheGenIrs972275
hapmaprs972275
1000 genomesrs972275
hgdprs972275
ensemblrs972275
gopubmedrs972275
geneviewrs972275
scholarrs972275
googlers972275
pharmgkbrs972275
gwascentralrs972275
openSNPrs972275
23andMers972275
23andMe allrs972275
SNP Nexus

SNPshotrs972275
SNPdbers972275
MSV3drs972275
GWAS Ctlgrs972275
GMAF0.4389
Max Magnitude0
? (C;C) (C;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
rs972275
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary