rs191564916

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common genotype

Make rs191564916(A;G)

Make rs191564916(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

18

Position

31524877

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs191564916
dbSNP (classic)	rs191564916
ClinGen	rs191564916
ebi	rs191564916
HLI	rs191564916
Exac	rs191564916
Gnomad	rs191564916
Varsome	rs191564916
LitVar	rs191564916
Map	rs191564916
PheGenI	rs191564916
Biobank	rs191564916
1000 genomes	rs191564916
hgdp	rs191564916
ensembl	rs191564916
geneview	rs191564916
scholar	rs191564916
google	rs191564916
pharmgkb	rs191564916
gwascentral	rs191564916
openSNP	rs191564916
23andMe	rs191564916
SNPshot	rs191564916
SNPdbe	rs191564916
MSV3d	rs191564916
GWAS Ctlg	rs191564916

Max Magnitude

0

ClinVar
Risk	rs191564916(G;G)
Alt	rs191564916(G;G)
Reference	Rs191564916(A;A)
Significance	Other
Disease	not specified Arrhythmogenic right ventricular cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy Cardiovascular phenotype
Variation	info
Gene	DSG2
CLNDBN	not specified Arrhythmogenic right ventricular cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy, type 10 Cardiovascular phenotype
Reversed	0
HGVS	NC_000018.9:g.29104840A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000037261.6, RCV000157183.2, RCV000230234.2, RCV000252861.1,