rs34417028

Orientation

plus

Stabilized

plus

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

Make rs34417028(C;C)

Make rs34417028(C;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31546033

Gene	DSG2, DSG2-AS1

is a	snp
is	mentioned by
dbSNP	rs34417028
dbSNP (classic)	rs34417028
ClinGen	rs34417028
ebi	rs34417028
HLI	rs34417028
Exac	rs34417028
Gnomad	rs34417028
Varsome	rs34417028
LitVar	rs34417028
Map	rs34417028
PheGenI	rs34417028
Biobank	rs34417028
1000 genomes	rs34417028
hgdp	rs34417028
ensembl	rs34417028
geneview	rs34417028
scholar	rs34417028
google	rs34417028
pharmgkb	rs34417028
gwascentral	rs34417028
openSNP	rs34417028
23andMe	rs34417028
SNPshot	rs34417028
SNPdbe	rs34417028
MSV3d	rs34417028
GWAS Ctlg	rs34417028

GMAF

0.004132

Max Magnitude

0

ClinVar
Risk	rs34417028(C;C)
Alt	rs34417028(C;C)
Reference	Rs34417028(T;T)
Significance	Non-pathogenic
Disease	Cardiomyopathy not specified Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSG2-AS1 DSG2
CLNDBN	Cardiomyopathy not specified Arrhythmogenic right ventricular cardiomyopathy, type 10
Reversed	0
HGVS	NC_000018.9:g.29125996T>C
CLNSRC	ClinVar GeneDx LabCorp
CLNACC	RCV000029669.3, RCV000037291.3, RCV000460568.1,