rs1014867

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1014867(C;T)

Make rs1014867(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

125491736

Gene

FAT4

is a	snp
is	mentioned by
dbSNP	rs1014867
dbSNP (classic)	rs1014867
ClinGen	rs1014867
ebi	rs1014867
HLI	rs1014867
Exac	rs1014867
Gnomad	rs1014867
Varsome	rs1014867
LitVar	rs1014867
Map	rs1014867
PheGenI	rs1014867
Biobank	rs1014867
1000 genomes	rs1014867
hgdp	rs1014867
ensembl	rs1014867
geneview	rs1014867
scholar	rs1014867
google	rs1014867
pharmgkb	rs1014867
gwascentral	rs1014867
openSNP	rs1014867
23andMe	rs1014867
SNPshot	rs1014867
SNPdbe	rs1014867
MSV3d	rs1014867
GWAS Ctlg	rs1014867

GMAF

0.0652

Max Magnitude

0

?	(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,