rs1060500610

Orientation

plus

Stabilized

plus

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

Make rs1060500610(C;T)

Make rs1060500610(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

7581012

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs1060500610
dbSNP (classic)	rs1060500610
ClinGen	rs1060500610
ebi	rs1060500610
HLI	rs1060500610
Exac	rs1060500610
Gnomad	rs1060500610
Varsome	rs1060500610
LitVar	rs1060500610
Map	rs1060500610
PheGenI	rs1060500610
Biobank	rs1060500610
1000 genomes	rs1060500610
hgdp	rs1060500610
ensembl	rs1060500610
geneview	rs1060500610
scholar	rs1060500610
google	rs1060500610
pharmgkb	rs1060500610
gwascentral	rs1060500610
openSNP	rs1060500610
23andMe	rs1060500610
SNPshot	rs1060500610
SNPdbe	rs1060500610
MSV3d	rs1060500610
GWAS Ctlg	rs1060500610

Max Magnitude

0

ClinVar
Risk	rs1060500610(T;T)
Alt	rs1060500610(T;T)
Reference	Rs1060500610(C;C)
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.7581245C>T
CLNSRC
CLNACC	RCV000472826.1,