rs1057519836

Orientation

plus

Stabilized

plus

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

Make rs1057519836(A;C)

Make rs1057519836(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

41224630

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs1057519836
dbSNP (classic)	rs1057519836
ClinGen	rs1057519836
ebi	rs1057519836
HLI	rs1057519836
Exac	rs1057519836
Gnomad	rs1057519836
Varsome	rs1057519836
LitVar	rs1057519836
Map	rs1057519836
PheGenI	rs1057519836
Biobank	rs1057519836
1000 genomes	rs1057519836
hgdp	rs1057519836
ensembl	rs1057519836
geneview	rs1057519836
scholar	rs1057519836
google	rs1057519836
pharmgkb	rs1057519836
gwascentral	rs1057519836
openSNP	rs1057519836
23andMe	rs1057519836
SNPshot	rs1057519836
SNPdbe	rs1057519836
MSV3d	rs1057519836
GWAS Ctlg	rs1057519836

Max Magnitude

0

ClinVar
Risk	rs1057519836(C;C) rs1057519836(G;G) rs1057519836(T;T)
Alt	rs1057519836(C;C) rs1057519836(G;G) rs1057519836(T;T)
Reference	Rs1057519836(A;A)
Significance	Probable-Pathogenic
Disease	Neoplasm Neoplasm of stomach
Variation	info
Gene	CTNNB1
CLNDBN	Neoplasm Neoplasm of stomach
Reversed	0
HGVS	NC_000003.11:g.41266121A>C; NC_000003.11:g.41266121A>G; NC_000003.11:g.41266121A>T
CLNSRC
CLNACC	RCV000425513.1, RCV000433725.1, RCV000444185.1,