rs185821167

Orientation

plus

Stabilized

plus

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

Make rs185821167(A;A)

Make rs185821167(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31524749

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs185821167
dbSNP (classic)	rs185821167
ClinGen	rs185821167
ebi	rs185821167
HLI	rs185821167
Exac	rs185821167
Gnomad	rs185821167
Varsome	rs185821167
LitVar	rs185821167
Map	rs185821167
PheGenI	rs185821167
Biobank	rs185821167
1000 genomes	rs185821167
hgdp	rs185821167
ensembl	rs185821167
geneview	rs185821167
scholar	rs185821167
google	rs185821167
pharmgkb	rs185821167
gwascentral	rs185821167
openSNP	rs185821167
23andMe	rs185821167
SNPshot	rs185821167
SNPdbe	rs185821167
MSV3d	rs185821167
GWAS Ctlg	rs185821167

Max Magnitude

0

ClinVar
Risk	rs185821167(A;A) rs185821167(T;T)
Alt	rs185821167(A;A) rs185821167(T;T)
Reference	Rs185821167(G;G)
Significance	Probable-Pathogenic
Disease	not specified Arrhythmogenic right ventricular cardiomyopathy not provided
Variation	info
Gene	DSG2
CLNDBN	not specified Arrhythmogenic right ventricular cardiomyopathy, type 10 not provided
Reversed	0
HGVS	NC_000018.9:g.29104712G>A; NC_000018.9:g.29104712G>T
CLNSRC
CLNACC	RCV000037318.3, RCV000205277.1, RCV000181210.1, RCV000465847.1,