rs587777135

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(CAA;CAA)	0	common in clinvar
(I;I)	0	common genotype
(TTG;TTG)	0	common in clinvar
(TTGG;TTGG)	0	common in clinvar

Make rs587777135(-;-)

Make rs587777135(-;CAA)

Reference

GRCh38 38.1/142

Chromosome

10

Position

65966714

Gene

CTNNA3

is a	snp
is	mentioned by
dbSNP	rs587777135
dbSNP (classic)	rs587777135
ClinGen	rs587777135
ebi	rs587777135
HLI	rs587777135
Exac	rs587777135
Gnomad	rs587777135
Varsome	rs587777135
LitVar	rs587777135
Map	rs587777135
PheGenI	rs587777135
Biobank	rs587777135
1000 genomes	rs587777135
hgdp	rs587777135
ensembl	rs587777135
geneview	rs587777135
scholar	rs587777135
google	rs587777135
pharmgkb	rs587777135
gwascentral	rs587777135
openSNP	rs587777135
23andMe	rs587777135
SNPshot	rs587777135
SNPdbe	rs587777135
MSV3d	rs587777135
GWAS Ctlg	rs587777135

Max Magnitude

0

ClinVar
Risk	Rs587777135(CAA;CAA) rs587777135(-;-)
Alt	Rs587777135(CAA;CAA) rs587777135(-;-)
Reference	Rs587777135(TTG;TTG)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular dysplasia Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	CTNNA3
CLNDBN	Arrhythmogenic right ventricular dysplasia, familial, 13 Arrhythmogenic right ventricular cardiomyopathy
Reversed	1
HGVS	NC_000010.10:g.67726472_67726474delCAA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000087057.3, RCV000487676.1,