rs397516923

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.7	Arrhythmogenic right ventricular dysplasia

Make rs397516923(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

7555761

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs397516923
dbSNP (classic)	rs397516923
ClinGen	rs397516923
ebi	rs397516923
HLI	rs397516923
Exac	rs397516923
Gnomad	rs397516923
Varsome	rs397516923
LitVar	rs397516923
Map	rs397516923
PheGenI	rs397516923
Biobank	rs397516923
1000 genomes	rs397516923
hgdp	rs397516923
ensembl	rs397516923
geneview	rs397516923
scholar	rs397516923
google	rs397516923
pharmgkb	rs397516923
gwascentral	rs397516923
openSNP	rs397516923
23andMe	rs397516923
SNPshot	rs397516923
SNPdbe	rs397516923
MSV3d	rs397516923
GWAS Ctlg	rs397516923

Max Magnitude

6.7

ClinVar
Risk	rs397516923(T;T)
Alt	rs397516923(T;T)
Reference	Rs397516923(C;C)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSP
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy
Reversed	0
HGVS	NC_000006.11:g.7555994C>T
CLNSRC	ClinVar
CLNACC	RCV000038006.2,