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rs1014867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1014867(C;T)
Make rs1014867(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position125491736
GeneFAT4
is asnp
is mentioned by
dbSNPrs1014867
dbSNP (old)rs1014867
ClinGenrs1014867
ebirs1014867
HLIrs1014867
Exacrs1014867
Gnomadrs1014867
Varsomers1014867
Maprs1014867
PheGenIrs1014867
Biobankrs1014867
1000 genomesrs1014867
hgdprs1014867
ensemblrs1014867
gopubmedrs1014867
geneviewrs1014867
scholarrs1014867
googlers1014867
pharmgkbrs1014867
gwascentralrs1014867
openSNPrs1014867
23andMers1014867
23andMe allrs1014867
SNP Nexus

SNPshotrs1014867
SNPdbers1014867
MSV3drs1014867
GWAS Ctlgrs1014867
GMAF0.0652
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 rs1014867(T;T)
Alt rs1014867(T;T)
Reference Rs1014867(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene FAT4
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.126412891C>T
CLNSRC
CLNACC RCV000428726.1,