rs267606674

Orientation

minus

Stabilized

minus

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

Make rs267606674(-;-)

Make rs267606674(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

65536467

Gene

AXIN2

is a	snp
is	mentioned by
dbSNP	rs267606674
dbSNP (classic)	rs267606674
ClinGen	rs267606674
ebi	rs267606674
HLI	rs267606674
Exac	rs267606674
Gnomad	rs267606674
Varsome	rs267606674
LitVar	rs267606674
Map	rs267606674
PheGenI	rs267606674
Biobank	rs267606674
1000 genomes	rs267606674
hgdp	rs267606674
ensembl	rs267606674
geneview	rs267606674
scholar	rs267606674
google	rs267606674
pharmgkb	rs267606674
gwascentral	rs267606674
openSNP	rs267606674
23andMe	rs267606674
SNPshot	rs267606674
SNPdbe	rs267606674
MSV3d	rs267606674
GWAS Ctlg	rs267606674

Max Magnitude

0

ClinVar
Risk	rs267606674(-;-)
Alt	rs267606674(-;-)
Reference	Rs267606674(G;G)
Significance	Pathogenic
Disease	Carcinoma of colon Oligodontia-colorectal cancer syndrome
Variation	info
Gene	AXIN2
CLNDBN	Carcinoma of colon Oligodontia-colorectal cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.63532585delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006238.4, RCV000463233.1,