rs727503741

Orientation

plus

Stabilized

plus

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

Make rs727503741(C;T)

Make rs727503741(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

74114349

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs727503741
dbSNP (classic)	rs727503741
ClinGen	rs727503741
ebi	rs727503741
HLI	rs727503741
Exac	rs727503741
Gnomad	rs727503741
Varsome	rs727503741
LitVar	rs727503741
Map	rs727503741
PheGenI	rs727503741
Biobank	rs727503741
1000 genomes	rs727503741
hgdp	rs727503741
ensembl	rs727503741
geneview	rs727503741
scholar	rs727503741
google	rs727503741
pharmgkb	rs727503741
gwascentral	rs727503741
openSNP	rs727503741
23andMe	rs727503741
SNPshot	rs727503741
SNPdbe	rs727503741
MSV3d	rs727503741
GWAS Ctlg	rs727503741

Max Magnitude

0

ClinVar
Risk	rs727503741(T;T)
Alt	rs727503741(T;T)
Reference	Rs727503741(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75874107C>T
CLNSRC
CLNACC	RCV000152653.1,