rs1039808

Orientation

minus

Stabilized

minus

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

Make rs1039808(A;A)

Make rs1039808(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

125318831

Gene

FAT4

is a	snp
is	mentioned by
dbSNP	rs1039808
dbSNP (classic)	rs1039808
ClinGen	rs1039808
ebi	rs1039808
HLI	rs1039808
Exac	rs1039808
Gnomad	rs1039808
Varsome	rs1039808
LitVar	rs1039808
Map	rs1039808
PheGenI	rs1039808
Biobank	rs1039808
1000 genomes	rs1039808
hgdp	rs1039808
ensembl	rs1039808
geneview	rs1039808
scholar	rs1039808
google	rs1039808
pharmgkb	rs1039808
gwascentral	rs1039808
openSNP	rs1039808
23andMe	rs1039808
SNPshot	rs1039808
SNPdbe	rs1039808
MSV3d	rs1039808
GWAS Ctlg	rs1039808

GMAF

0.4141

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

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

ClinVar
Risk	rs1039808(A;A) rs1039808(C;C)
Alt	rs1039808(A;A) rs1039808(C;C)
Reference	Rs1039808(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	FAT4
CLNDBN	not specified
Reversed	1
HGVS	NC_000004.11:g.126239986C>T
CLNSRC
CLNACC	RCV000433556.1,