rs878853170

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.7	Arrhythmogenic right ventricular dysplasia

Make rs878853170(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

18

Position

31079850

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs878853170
dbSNP (classic)	rs878853170
ClinGen	rs878853170
ebi	rs878853170
HLI	rs878853170
Exac	rs878853170
Gnomad	rs878853170
Varsome	rs878853170
LitVar	rs878853170
Map	rs878853170
PheGenI	rs878853170
Biobank	rs878853170
1000 genomes	rs878853170
hgdp	rs878853170
ensembl	rs878853170
geneview	rs878853170
scholar	rs878853170
google	rs878853170
pharmgkb	rs878853170
gwascentral	rs878853170
openSNP	rs878853170
23andMe	rs878853170
SNPshot	rs878853170
SNPdbe	rs878853170
MSV3d	rs878853170
GWAS Ctlg	rs878853170

Max Magnitude

6.7

ClinVar
Risk	rs878853170(T;T)
Alt	rs878853170(T;T)
Reference	Rs878853170(C;C)
Significance	Pathogenic
Disease	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA not provided
Variation	info
Gene	DSC2
CLNDBN	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH OR WITHOUT MILD PALMOPLANTAR KERATODERMA not provided
Reversed	1
HGVS	NC_000018.9:g.28659816G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000224990.1, RCV000254959.2,