rs797044875

Orientation

plus

Stabilized

plus

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

Make rs797044875(A;A)

Make rs797044875(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

41235763

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs797044875
dbSNP (classic)	rs797044875
ClinGen	rs797044875
ebi	rs797044875
HLI	rs797044875
Exac	rs797044875
Gnomad	rs797044875
Varsome	rs797044875
LitVar	rs797044875
Map	rs797044875
PheGenI	rs797044875
Biobank	rs797044875
1000 genomes	rs797044875
hgdp	rs797044875
ensembl	rs797044875
geneview	rs797044875
scholar	rs797044875
google	rs797044875
pharmgkb	rs797044875
gwascentral	rs797044875
openSNP	rs797044875
23andMe	rs797044875
SNPshot	rs797044875
SNPdbe	rs797044875
MSV3d	rs797044875
GWAS Ctlg	rs797044875

Max Magnitude

0

ClinVar
Risk	rs797044875(A;A)
Alt	rs797044875(A;A)
Reference	Rs797044875(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	CTNNB1
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000003.11:g.41277254G>A
CLNSRC
CLNACC	RCV000190686.1,