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rs28362459

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28362459(G;G)
Make rs28362459(G;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position5844781
GeneFUT3
is asnp
is mentioned by
dbSNPrs28362459
ebirs28362459
HLIrs28362459
Exacrs28362459
Varsomers28362459
Maprs28362459
PheGenIrs28362459
hapmaprs28362459
1000 genomesrs28362459
hgdprs28362459
ensemblrs28362459
gopubmedrs28362459
geneviewrs28362459
scholarrs28362459
googlers28362459
pharmgkbrs28362459
gwascentralrs28362459
openSNPrs28362459
23andMers28362459
23andMe allrs28362459
SNP Nexus

SNPshotrs28362459
SNPdbers28362459
MSV3drs28362459
GWAS Ctlgrs28362459
GMAF0.2089
Max Magnitude0
OMIM111100
DescLe(-) PHENOTYPE
Variant0001
Relatedalso


ClinVar
Risk rs28362459(G;G)
Alt rs28362459(G;G)
Reference rs28362459(T;T)
Significance Other
Disease Le(-) PHENOTYPE
Variation info
Gene FUT3
CLNDBN Le(-) PHENOTYPE
Reversed 1
HGVS NC_000019.9:g.5844792A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019289.23,



[PMID 19169360OA-icon.png] Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity.


GET Evidence
FUT3-L20R
aa_change Leu20Arg
aa_change_short L20R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.16084
summary