rs1133683

Orientation

minus

Stabilized

minus

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

Make rs1133683(C;T)

Make rs1133683(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

65537650

Gene

AXIN2

is a	snp
is	mentioned by
dbSNP	rs1133683
dbSNP (classic)	rs1133683
ClinGen	rs1133683
ebi	rs1133683
HLI	rs1133683
Exac	rs1133683
Gnomad	rs1133683
Varsome	rs1133683
LitVar	rs1133683
Map	rs1133683
PheGenI	rs1133683
Biobank	rs1133683
1000 genomes	rs1133683
hgdp	rs1133683
ensembl	rs1133683
geneview	rs1133683
scholar	rs1133683
google	rs1133683
pharmgkb	rs1133683
gwascentral	rs1133683
openSNP	rs1133683
23andMe	rs1133683
SNPshot	rs1133683
SNPdbe	rs1133683
MSV3d	rs1133683
GWAS Ctlg	rs1133683

GMAF

0.449

Max Magnitude

0

[PMID 21069480] AXIN2 polymorphism and its association with prostate cancer in a Turkish population

ClinVar
Risk	rs1133683(T;T)
Alt	rs1133683(T;T)
Reference	Rs1133683(C;C)
Significance	Non-pathogenic
Disease	not specified Oligodontia-colorectal cancer syndrome
Variation	info
Gene	AXIN2
CLNDBN	not specified Oligodontia-colorectal cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.63533768G>A
CLNSRC
CLNACC	RCV000253379.1, RCV000302412.1,