rs397516915

Orientation

plus

Stabilized

plus

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

Make rs397516915(C;T)

Make rs397516915(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

7568443

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs397516915
dbSNP (classic)	rs397516915
ClinGen	rs397516915
ebi	rs397516915
HLI	rs397516915
Exac	rs397516915
Gnomad	rs397516915
Varsome	rs397516915
LitVar	rs397516915
Map	rs397516915
PheGenI	rs397516915
Biobank	rs397516915
1000 genomes	rs397516915
hgdp	rs397516915
ensembl	rs397516915
geneview	rs397516915
scholar	rs397516915
google	rs397516915
pharmgkb	rs397516915
gwascentral	rs397516915
openSNP	rs397516915
23andMe	rs397516915
SNPshot	rs397516915
SNPdbe	rs397516915
MSV3d	rs397516915
GWAS Ctlg	rs397516915

Max Magnitude

0

ClinVar
Risk	rs397516915(T;T)
Alt	rs397516915(T;T)
Reference	Rs397516915(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.7568676C>T
CLNSRC	ClinVar
CLNACC	RCV000208168.2,