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rs1567047

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1567047(C;T)
Make rs1567047(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position125451587
GeneFAT4
is asnp
is mentioned by
dbSNPrs1567047
dbSNP (classic)rs1567047
ClinGenrs1567047
ebirs1567047
HLIrs1567047
Exacrs1567047
Gnomadrs1567047
Varsomers1567047
LitVarrs1567047
Maprs1567047
PheGenIrs1567047
Biobankrs1567047
1000 genomesrs1567047
hgdprs1567047
ensemblrs1567047
geneviewrs1567047
scholarrs1567047
googlers1567047
pharmgkbrs1567047
gwascentralrs1567047
openSNPrs1567047
23andMers1567047
SNPshotrs1567047
SNPdbers1567047
MSV3drs1567047
GWAS Ctlgrs1567047
GMAF0.2585
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23319386] Nonsynonymous polymorphisms in FAT4 gene are associated with the risk of esophageal cancer in an Eastern Chinese population


ClinVar
Risk rs1567047(T;T)
Alt rs1567047(T;T)
Reference Rs1567047(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene FAT4
CLNDBN not specified
Reversed 1
HGVS NC_000004.11:g.126372742G>A
CLNSRC
CLNACC RCV000427798.1,