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rs4855271

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(T;T) 0 common on affy axiom data
Make rs4855271(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position164996744
GeneSI
is asnp
is mentioned by
dbSNPrs4855271
dbSNP (classic)rs4855271
ClinGenrs4855271
ebirs4855271
HLIrs4855271
Exacrs4855271
Gnomadrs4855271
Varsomers4855271
LitVarrs4855271
Maprs4855271
PheGenIrs4855271
Biobankrs4855271
1000 genomesrs4855271
hgdprs4855271
ensemblrs4855271
geneviewrs4855271
scholarrs4855271
googlers4855271
pharmgkbrs4855271
gwascentralrs4855271
openSNPrs4855271
23andMers4855271
SNPshotrs4855271
SNPdbers4855271
MSV3drs4855271
GWAS Ctlgrs4855271
GMAF0.07438
Max Magnitude0
? (C;C) (C;T) (T;T) 28




ClinVar
Risk Rs4855271(T;T)
Alt Rs4855271(T;T)
Reference Rs4855271(C;C)
Significance Non-pathogenic
Disease Sucrase-isomaltase deficiency
Variation info
Gene SI
CLNDBN Sucrase-isomaltase deficiency
Reversed 0
HGVS NC_000003.11:g.164714532C>T
CLNSRC
CLNACC RCV000394925.1,