rs876657674

Orientation

plus

Stabilized

plus

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

Make rs876657674(-;G)

Make rs876657674(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

74074790

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs876657674
dbSNP (classic)	rs876657674
ClinGen	rs876657674
ebi	rs876657674
HLI	rs876657674
Exac	rs876657674
Gnomad	rs876657674
Varsome	rs876657674
LitVar	rs876657674
Map	rs876657674
PheGenI	rs876657674
Biobank	rs876657674
1000 genomes	rs876657674
hgdp	rs876657674
ensembl	rs876657674
geneview	rs876657674
scholar	rs876657674
google	rs876657674
pharmgkb	rs876657674
gwascentral	rs876657674
openSNP	rs876657674
23andMe	rs876657674
SNPshot	rs876657674
SNPdbe	rs876657674
MSV3d	rs876657674
GWAS Ctlg	rs876657674

Max Magnitude

0

ClinVar
Risk	rs876657674(G;G)
Alt	rs876657674(G;G)
Reference	Rs876657674(-;-)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75834548dupG
CLNSRC
CLNACC	RCV000221392.1,