rs1060500609

Orientation

plus

Stabilized

plus

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

Make rs1060500609(G;T)

Make rs1060500609(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

7569185

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs1060500609
dbSNP (classic)	rs1060500609
ClinGen	rs1060500609
ebi	rs1060500609
HLI	rs1060500609
Exac	rs1060500609
Gnomad	rs1060500609
Varsome	rs1060500609
LitVar	rs1060500609
Map	rs1060500609
PheGenI	rs1060500609
Biobank	rs1060500609
1000 genomes	rs1060500609
hgdp	rs1060500609
ensembl	rs1060500609
geneview	rs1060500609
scholar	rs1060500609
google	rs1060500609
pharmgkb	rs1060500609
gwascentral	rs1060500609
openSNP	rs1060500609
23andMe	rs1060500609
SNPshot	rs1060500609
SNPdbe	rs1060500609
MSV3d	rs1060500609
GWAS Ctlg	rs1060500609

Max Magnitude

0

ClinVar
Risk	rs1060500609(T;T)
Alt	rs1060500609(T;T)
Reference	Rs1060500609(G;G)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSP
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy, type 8
Reversed	0
HGVS	NC_000006.11:g.7569418G>T
CLNSRC
CLNACC	RCV000465188.1,