rs9915936

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(T;T)	0	common in clinvar

Make rs9915936(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

65537671

Gene

AXIN2

is a	snp
is	mentioned by
dbSNP	rs9915936
dbSNP (classic)	rs9915936
ClinGen	rs9915936
ebi	rs9915936
HLI	rs9915936
Exac	rs9915936
Gnomad	rs9915936
Varsome	rs9915936
LitVar	rs9915936
Map	rs9915936
PheGenI	rs9915936
Biobank	rs9915936
1000 genomes	rs9915936
hgdp	rs9915936
ensembl	rs9915936
geneview	rs9915936
scholar	rs9915936
google	rs9915936
pharmgkb	rs9915936
gwascentral	rs9915936
openSNP	rs9915936
23andMe	rs9915936
SNPshot	rs9915936
SNPdbe	rs9915936
MSV3d	rs9915936
GWAS Ctlg	rs9915936

GMAF

0.1097

Max Magnitude

0

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

ClinVar
Risk	Rs9915936(C;C)
Alt	Rs9915936(C;C)
Reference	Rs9915936(T;T)
Significance	Non-pathogenic
Disease	not specified Oligodontia-colorectal cancer syndrome
Variation	info
Gene	AXIN2
CLNDBN	not specified Oligodontia-colorectal cancer syndrome
Reversed	0
HGVS	NC_000017.10:g.63533789T>C
CLNSRC
CLNACC	RCV000250428.1, RCV000305836.1,