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rs2430212

From SNPedia

Orientationplus
Stabilizedplus
Make rs2430212(C;C)
Make rs2430212(C;T)
Make rs2430212(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position117954093
GeneKLHL13
is asnp
is mentioned by
dbSNPrs2430212
ebirs2430212
HLIrs2430212
Exacrs2430212
Varsomers2430212
Maprs2430212
PheGenIrs2430212
hapmaprs2430212
1000 genomesrs2430212
hgdprs2430212
ensemblrs2430212
gopubmedrs2430212
geneviewrs2430212
scholarrs2430212
googlers2430212
pharmgkbrs2430212
gwascentralrs2430212
openSNPrs2430212
23andMers2430212
23andMe allrs2430212
SNP Nexus

SNPshotrs2430212
SNPdbers2430212
MSV3drs2430212
GWAS Ctlgrs2430212
GMAF0.416
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 0.000002
Odds Ratio NR NR



GET Evidence
rs2430212
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.597826
summary