rs863224864

Orientation

plus

Stabilized

plus

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

Make rs863224864(G;G)

Make rs863224864(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

41233614

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs863224864
dbSNP (classic)	rs863224864
ClinGen	rs863224864
ebi	rs863224864
HLI	rs863224864
Exac	rs863224864
Gnomad	rs863224864
Varsome	rs863224864
LitVar	rs863224864
Map	rs863224864
PheGenI	rs863224864
Biobank	rs863224864
1000 genomes	rs863224864
hgdp	rs863224864
ensembl	rs863224864
geneview	rs863224864
scholar	rs863224864
google	rs863224864
pharmgkb	rs863224864
gwascentral	rs863224864
openSNP	rs863224864
23andMe	rs863224864
SNPshot	rs863224864
SNPdbe	rs863224864
MSV3d	rs863224864
GWAS Ctlg	rs863224864

Max Magnitude

0

ClinVar
Risk	rs863224864(G;G)
Alt	rs863224864(G;G)
Reference	Rs863224864(T;T)
Significance	Probable-Pathogenic
Disease	Mental retardation
Variation	info
Gene	CTNNB1
CLNDBN	Mental retardation, autosomal dominant 19
Reversed	0
HGVS	NC_000003.11:g.41275105T>G
CLNSRC
CLNACC	RCV000199502.1,