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rs2280673

From SNPedia

Orientationplus
Stabilizedplus
Make rs2280673(A;A)
Make rs2280673(A;C)
Make rs2280673(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position133839310
GeneRAB6B
is asnp
is mentioned by
dbSNPrs2280673
ebirs2280673
HLIrs2280673
Exacrs2280673
Varsomers2280673
Maprs2280673
PheGenIrs2280673
hapmaprs2280673
1000 genomesrs2280673
hgdprs2280673
ensemblrs2280673
gopubmedrs2280673
geneviewrs2280673
scholarrs2280673
googlers2280673
pharmgkbrs2280673
gwascentralrs2280673
openSNPrs2280673
23andMers2280673
23andMe allrs2280673
SNP Nexus

SNPshotrs2280673
SNPdbers2280673
MSV3drs2280673
GWAS Ctlgrs2280673
GMAF0.4408
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 19084217OA-icon.png] Relevant to Hemochromatosis
OMIM190000
DescTRANSFERRIN; TF
Variant
Relatedalso



GET Evidence
rs2280673
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.546875
summary



[PMID 26597663] Genetic factors influencing ferritin levels in 14,126 blood donors: results from the Danish Blood Donor Study