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rs932316

From SNPedia

Orientationplus
Stabilizedplus
Make rs932316(C;C)
Make rs932316(C;T)
Make rs932316(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position25640972
is asnp
is mentioned by
dbSNPrs932316
ebirs932316
HLIrs932316
Exacrs932316
Varsomers932316
Maprs932316
PheGenIrs932316
hapmaprs932316
1000 genomesrs932316
hgdprs932316
ensemblrs932316
gopubmedrs932316
geneviewrs932316
scholarrs932316
googlers932316
pharmgkbrs932316
gwascentralrs932316
openSNPrs932316
23andMers932316
23andMe allrs932316
SNP Nexus

SNPshotrs932316
SNPdbers932316
MSV3drs932316
GWAS Ctlgrs932316
GMAF0.1754
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 0.000009
Odds Ratio NR NR



GET Evidence
rs932316
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary