rs786204291

Orientation

plus

Stabilized

plus

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

Make rs786204291(A;G)

Make rs786204291(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

31522152

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs786204291
dbSNP (classic)	rs786204291
ClinGen	rs786204291
ebi	rs786204291
HLI	rs786204291
Exac	rs786204291
Gnomad	rs786204291
Varsome	rs786204291
LitVar	rs786204291
Map	rs786204291
PheGenI	rs786204291
Biobank	rs786204291
1000 genomes	rs786204291
hgdp	rs786204291
ensembl	rs786204291
geneview	rs786204291
scholar	rs786204291
google	rs786204291
pharmgkb	rs786204291
gwascentral	rs786204291
openSNP	rs786204291
23andMe	rs786204291
SNPshot	rs786204291
SNPdbe	rs786204291
MSV3d	rs786204291
GWAS Ctlg	rs786204291

Max Magnitude

0

ClinVar
Risk	rs786204291(G;G)
Alt	rs786204291(G;G)
Reference	Rs786204291(A;A)
Significance	Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	DSG2
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000018.9:g.29102115A>G
CLNSRC
CLNACC	RCV000168630.2, RCV000414987.1,