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rs973968

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs973968(A;G)
Make rs973968(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position62187980
is asnp
is mentioned by
dbSNPrs973968
ebirs973968
HLIrs973968
Exacrs973968
Varsomers973968
Maprs973968
PheGenIrs973968
hapmaprs973968
1000 genomesrs973968
hgdprs973968
ensemblrs973968
gopubmedrs973968
geneviewrs973968
scholarrs973968
googlers973968
pharmgkbrs973968
gwascentralrs973968
openSNPrs973968
23andMers973968
23andMe allrs973968
SNP Nexus

SNPshotrs973968
SNPdbers973968
MSV3drs973968
GWAS Ctlgrs973968
GMAF0.1451
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 0.000003
Odds Ratio NR NR



GET Evidence
rs973968
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.835938
summary