rs62636492

Orientation

plus

Stabilized

plus

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

Make rs62636492(C;T)

Make rs62636492(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

219421364

Gene

DES

is a	snp
is	mentioned by
dbSNP	rs62636492
dbSNP (classic)	rs62636492
ClinGen	rs62636492
ebi	rs62636492
HLI	rs62636492
Exac	rs62636492
Gnomad	rs62636492
Varsome	rs62636492
LitVar	rs62636492
Map	rs62636492
PheGenI	rs62636492
Biobank	rs62636492
1000 genomes	rs62636492
hgdp	rs62636492
ensembl	rs62636492
geneview	rs62636492
scholar	rs62636492
google	rs62636492
pharmgkb	rs62636492
gwascentral	rs62636492
openSNP	rs62636492
23andMe	rs62636492
SNPshot	rs62636492
SNPdbe	rs62636492
MSV3d	rs62636492
GWAS Ctlg	rs62636492

Max Magnitude

0

ClinVar
Risk	rs62636492(T;T)
Alt	rs62636492(T;T)
Reference	Rs62636492(C;C)
Significance	Probable-Pathogenic
Disease	not specified not provided Primary dilated cardiomyopathy
Variation	info
Gene	DES
CLNDBN	not specified not provided Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000002.11:g.220286086C>T
CLNSRC
CLNACC	RCV000037224.2, RCV000056766.1, RCV000157164.1,