rs869312766

Orientation

plus

Stabilized

plus

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

Make rs869312766(-;-)

Make rs869312766(-;TGAA)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

138783266

Gene

CTNNA1

is a	snp
is	mentioned by
dbSNP	rs869312766
dbSNP (classic)	rs869312766
ClinGen	rs869312766
ebi	rs869312766
HLI	rs869312766
Exac	rs869312766
Gnomad	rs869312766
Varsome	rs869312766
LitVar	rs869312766
Map	rs869312766
PheGenI	rs869312766
Biobank	rs869312766
1000 genomes	rs869312766
hgdp	rs869312766
ensembl	rs869312766
geneview	rs869312766
scholar	rs869312766
google	rs869312766
pharmgkb	rs869312766
gwascentral	rs869312766
openSNP	rs869312766
23andMe	rs869312766
SNPshot	rs869312766
SNPdbe	rs869312766
MSV3d	rs869312766
GWAS Ctlg	rs869312766

Max Magnitude

0

ClinVar
Risk	rs869312766(-;-)
Alt	rs869312766(-;-)
Reference	Rs869312766(TGAA;TGAA)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CTNNA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.138118955_138118958delTGAA
CLNSRC
CLNACC	RCV000210185.1,