rs727503738

Orientation

plus

Stabilized

plus

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

Make rs727503738(A;G)

Make rs727503738(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

74095654

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs727503738
dbSNP (classic)	rs727503738
ClinGen	rs727503738
ebi	rs727503738
HLI	rs727503738
Exac	rs727503738
Gnomad	rs727503738
Varsome	rs727503738
LitVar	rs727503738
Map	rs727503738
PheGenI	rs727503738
Biobank	rs727503738
1000 genomes	rs727503738
hgdp	rs727503738
ensembl	rs727503738
geneview	rs727503738
scholar	rs727503738
google	rs727503738
pharmgkb	rs727503738
gwascentral	rs727503738
openSNP	rs727503738
23andMe	rs727503738
SNPshot	rs727503738
SNPdbe	rs727503738
MSV3d	rs727503738
GWAS Ctlg	rs727503738

Max Magnitude

0

ClinVar
Risk	rs727503738(G;G)
Alt	rs727503738(G;G)
Reference	Rs727503738(A;A)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75855412A>G
CLNSRC
CLNACC	RCV000152646.1,