rs121913399

Orientation

plus

Stabilized

plus

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

Make rs121913399(A;A)

Make rs121913399(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

41224612

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs121913399
dbSNP (classic)	rs121913399
ClinGen	rs121913399
ebi	rs121913399
HLI	rs121913399
Exac	rs121913399
Gnomad	rs121913399
Varsome	rs121913399
LitVar	rs121913399
Map	rs121913399
PheGenI	rs121913399
Biobank	rs121913399
1000 genomes	rs121913399
hgdp	rs121913399
ensembl	rs121913399
geneview	rs121913399
scholar	rs121913399
google	rs121913399
pharmgkb	rs121913399
gwascentral	rs121913399
openSNP	rs121913399
23andMe	rs121913399
SNPshot	rs121913399
SNPdbe	rs121913399
MSV3d	rs121913399
GWAS Ctlg	rs121913399

Max Magnitude

0

ClinVar
Risk	rs121913399(A;A) rs121913399(C;C)
Alt	rs121913399(A;A) rs121913399(C;C)
Reference	Rs121913399(G;G)
Significance	Probable-Pathogenic
Disease	Craniopharyngioma Pilomatrixoma Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Malignant melanoma of skin Adenocarcinoma of lung Malignant neoplasm of body of uterus Medulloblastoma Adrenocortical carcinoma
Variation	info
Gene	CTNNB1
CLNDBN	Craniopharyngioma Pilomatrixoma Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Malignant melanoma of skin Adenocarcinoma of lung Malignant neoplasm of body of uterus Medulloblastoma Adrenocortical carcinoma
Reversed	0
HGVS	NC_000003.11:g.41266103G>A; NC_000003.11:g.41266103G>C
CLNSRC
CLNACC	RCV000426895.1, RCV000444074.1, RCV000418083.1, RCV000419419.1, RCV000420040.1, RCV000427501.1, RCV000427907.1, RCV000430713.1, RCV000436663.1, RCV000438184.1, RCV000438599.1, RCV000438776.1,