rs1060500613

Orientation

plus

Stabilized

plus

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

Make rs1060500613(-;-)

Make rs1060500613(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

7571564

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs1060500613
dbSNP (classic)	rs1060500613
ClinGen	rs1060500613
ebi	rs1060500613
HLI	rs1060500613
Exac	rs1060500613
Gnomad	rs1060500613
Varsome	rs1060500613
LitVar	rs1060500613
Map	rs1060500613
PheGenI	rs1060500613
Biobank	rs1060500613
1000 genomes	rs1060500613
hgdp	rs1060500613
ensembl	rs1060500613
geneview	rs1060500613
scholar	rs1060500613
google	rs1060500613
pharmgkb	rs1060500613
gwascentral	rs1060500613
openSNP	rs1060500613
23andMe	rs1060500613
SNPshot	rs1060500613
SNPdbe	rs1060500613
MSV3d	rs1060500613
GWAS Ctlg	rs1060500613

Max Magnitude

0

ClinVar
Risk	rs1060500613(-;-)
Alt	rs1060500613(-;-)
Reference	Rs1060500613(G;G)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSP
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy, type 8
Reversed	0
HGVS	NC_000006.11:g.7571797delG
CLNSRC
CLNACC	RCV000468365.1,