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rs13194491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs13194491(C;T)
Make rs13194491(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position27069301
is asnp
is mentioned by
dbSNPrs13194491
ebirs13194491
HLIrs13194491
Exacrs13194491
Varsomers13194491
Maprs13194491
PheGenIrs13194491
hapmaprs13194491
1000 genomesrs13194491
hgdprs13194491
ensemblrs13194491
gopubmedrs13194491
geneviewrs13194491
scholarrs13194491
googlers13194491
pharmgkbrs13194491
gwascentralrs13194491
openSNPrs13194491
23andMers13194491
23andMe allrs13194491
SNP Nexus

SNPshotrs13194491
SNPdbers13194491
MSV3drs13194491
GWAS Ctlgrs13194491
GMAF0.03076
Max Magnitude0
? (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 1E-8
Odds Ratio NR NR



GET Evidence
rs13194491
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0234375
summary



[PMID 26460247] Genetic contribution to iron status: SNPs related to iron deficiency anaemia and fine mapping of CACNA2D3 calcium channel subunit