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rs4855271

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs4855271(C;C)
Make rs4855271(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position164996744
GeneSI
is asnp
is mentioned by
dbSNPrs4855271
ebirs4855271
HLIrs4855271
Exacrs4855271
Varsomers4855271
Maprs4855271
PheGenIrs4855271
hapmaprs4855271
1000 genomesrs4855271
hgdprs4855271
ensemblrs4855271
gopubmedrs4855271
geneviewrs4855271
scholarrs4855271
googlers4855271
pharmgkbrs4855271
gwascentralrs4855271
openSNPrs4855271
23andMers4855271
23andMe allrs4855271
SNP Nexus

SNPshotrs4855271
SNPdbers4855271
MSV3drs4855271
GWAS Ctlgrs4855271
GMAF0.07438
Max Magnitude0
? (C;C) (C;T) (T;T) 28
Venter snp
Source plos
Gene SI
allele T
frequency 0.933
sift
HuRef 1103656286251
Disease Association Defects in SI are the cause of disaccharide intolerance I (MIM:222900).



GET Evidence
SI-M1523I
aa_change Met1523Ile
aa_change_short M1523I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.923423
summary