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rs13188386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs13188386(A;A)
Make rs13188386(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position42473453
GeneGHR
is asnp
is mentioned by
dbSNPrs13188386
ebirs13188386
HLIrs13188386
Exacrs13188386
Varsomers13188386
Maprs13188386
PheGenIrs13188386
hapmaprs13188386
1000 genomesrs13188386
hgdprs13188386
ensemblrs13188386
gopubmedrs13188386
geneviewrs13188386
scholarrs13188386
googlers13188386
pharmgkbrs13188386
gwascentralrs13188386
openSNPrs13188386
23andMers13188386
23andMe allrs13188386
SNP Nexus

SNPshotrs13188386
SNPdbers13188386
MSV3drs13188386
GWAS Ctlgrs13188386
GMAF0.2264
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 0.000008
Odds Ratio NR NR



GET Evidence
rs13188386
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.328125
summary