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rs2052550

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2052550(A;A)
Make rs2052550(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position78977119
GeneARSB
is asnp
is mentioned by
dbSNPrs2052550
ebirs2052550
HLIrs2052550
Exacrs2052550
Varsomers2052550
Maprs2052550
PheGenIrs2052550
hapmaprs2052550
1000 genomesrs2052550
hgdprs2052550
ensemblrs2052550
gopubmedrs2052550
geneviewrs2052550
scholarrs2052550
googlers2052550
pharmgkbrs2052550
gwascentralrs2052550
openSNPrs2052550
23andMers2052550
23andMe allrs2052550
SNP Nexus

SNPshotrs2052550
SNPdbers2052550
MSV3drs2052550
GWAS Ctlgrs2052550
GMAF0.4885
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
rs2052550
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484375
summary