rs8081536

Orientation

plus

Stabilized

plus

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

Make rs8081536(C;T)

Make rs8081536(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

65538333

Gene

AXIN2

is a	snp
is	mentioned by
dbSNP	rs8081536
dbSNP (classic)	rs8081536
ClinGen	rs8081536
ebi	rs8081536
HLI	rs8081536
Exac	rs8081536
Gnomad	rs8081536
Varsome	rs8081536
LitVar	rs8081536
Map	rs8081536
PheGenI	rs8081536
Biobank	rs8081536
1000 genomes	rs8081536
hgdp	rs8081536
ensembl	rs8081536
geneview	rs8081536
scholar	rs8081536
google	rs8081536
pharmgkb	rs8081536
gwascentral	rs8081536
openSNP	rs8081536
23andMe	rs8081536
SNPshot	rs8081536
SNPdbe	rs8081536
MSV3d	rs8081536
GWAS Ctlg	rs8081536

GMAF

0.002755

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 19065536] [Association of single nucleotide polymorphisms of Axis inhibitor-2 gene rs224030, rs8081536, rs9913621 with Hirschsprung disease]

ClinVar
Risk	rs8081536(T;T)
Alt	rs8081536(T;T)
Reference	Rs8081536(C;C)
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.63534451C>T
CLNSRC
CLNACC	RCV000159770.4, RCV000232023.2,