rs1060500618

Orientation

plus

Stabilized

plus

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

Make rs1060500618(C;T)

Make rs1060500618(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

7575460

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs1060500618
dbSNP (classic)	rs1060500618
ClinGen	rs1060500618
ebi	rs1060500618
HLI	rs1060500618
Exac	rs1060500618
Gnomad	rs1060500618
Varsome	rs1060500618
LitVar	rs1060500618
Map	rs1060500618
PheGenI	rs1060500618
Biobank	rs1060500618
1000 genomes	rs1060500618
hgdp	rs1060500618
ensembl	rs1060500618
geneview	rs1060500618
scholar	rs1060500618
google	rs1060500618
pharmgkb	rs1060500618
gwascentral	rs1060500618
openSNP	rs1060500618
23andMe	rs1060500618
SNPshot	rs1060500618
SNPdbe	rs1060500618
MSV3d	rs1060500618
GWAS Ctlg	rs1060500618

Max Magnitude

0

ClinVar
Risk	rs1060500618(T;T)
Alt	rs1060500618(T;T)
Reference	Rs1060500618(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.7575693C>T
CLNSRC
CLNACC	RCV000460155.1,