rs377272752

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(D;D)	0	common genotype
(TCC;TCC)	0	common in clinvar

Make rs377272752(-;-)

Make rs377272752(-;CCT)

Make rs377272752(CCT;CCT)

Reference

GRCh38.p2 38.2/144

Chromosome

18

Position

31069032

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs377272752
dbSNP (classic)	rs377272752
ClinGen	rs377272752
ebi	rs377272752
HLI	rs377272752
Exac	rs377272752
Gnomad	rs377272752
Varsome	rs377272752
LitVar	rs377272752
Map	rs377272752
PheGenI	rs377272752
Biobank	rs377272752
1000 genomes	rs377272752
hgdp	rs377272752
ensembl	rs377272752
geneview	rs377272752
scholar	rs377272752
google	rs377272752
pharmgkb	rs377272752
gwascentral	rs377272752
openSNP	rs377272752
23andMe	rs377272752
SNPshot	rs377272752
SNPdbe	rs377272752
MSV3d	rs377272752
GWAS Ctlg	rs377272752

Merged from

Rs786205360

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs377272752(TCC;TCC)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy Cardiomyopathy
Variation	info
Gene	DSC2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy Cardiomyopathy
Reversed	0
HGVS	NC_000018.9:g.28648998_28649000delTCC
CLNSRC
CLNACC	RCV000157177.1, RCV000181173.1,