rs781036800

Orientation

plus

Stabilized

plus

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

Make rs781036800(-;-)

Make rs781036800(-;CT)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

74111991

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs781036800
dbSNP (classic)	rs781036800
ClinGen	rs781036800
ebi	rs781036800
HLI	rs781036800
Exac	rs781036800
Gnomad	rs781036800
Varsome	rs781036800
LitVar	rs781036800
Map	rs781036800
PheGenI	rs781036800
Biobank	rs781036800
1000 genomes	rs781036800
hgdp	rs781036800
ensembl	rs781036800
geneview	rs781036800
scholar	rs781036800
google	rs781036800
pharmgkb	rs781036800
gwascentral	rs781036800
openSNP	rs781036800
23andMe	rs781036800
SNPshot	rs781036800
SNPdbe	rs781036800
MSV3d	rs781036800
GWAS Ctlg	rs781036800

Max Magnitude

0

ClinVar
Risk	rs781036800(-;-)
Alt	rs781036800(-;-)
Reference	Rs781036800(CT;CT)
Significance	Probable-Pathogenic
Disease	not specified Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	not specified Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75871749_75871750delCT
CLNSRC
CLNACC	RCV000184003.2, RCV000219138.1,