rs121908567

Orientation

minus

Stabilized

minus

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

Make rs121908567(G;T)

Make rs121908567(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

65536345

Gene

AXIN2

is a	snp
is	mentioned by
dbSNP	rs121908567
dbSNP (classic)	rs121908567
ClinGen	rs121908567
ebi	rs121908567
HLI	rs121908567
Exac	rs121908567
Gnomad	rs121908567
Varsome	rs121908567
LitVar	rs121908567
Map	rs121908567
PheGenI	rs121908567
Biobank	rs121908567
1000 genomes	rs121908567
hgdp	rs121908567
ensembl	rs121908567
geneview	rs121908567
scholar	rs121908567
google	rs121908567
pharmgkb	rs121908567
gwascentral	rs121908567
openSNP	rs121908567
23andMe	rs121908567
SNPshot	rs121908567
SNPdbe	rs121908567
MSV3d	rs121908567
GWAS Ctlg	rs121908567

Max Magnitude

0

OMIM	604025
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908567(T;T)
Alt	rs121908567(T;T)
Reference	Rs121908567(G;G)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	AXIN2
CLNDBN	Carcinoma of colon
Reversed	1
HGVS	NC_000017.10:g.63532463C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006237.4,