rs397517245

Orientation

plus

Stabilized

plus

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

Make rs397517245(-;A)

Make rs397517245(A;A)

Reference

GRCh38 38.1/141

Chromosome

10

Position

74074779

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs397517245
dbSNP (classic)	rs397517245
ClinGen	rs397517245
ebi	rs397517245
HLI	rs397517245
Exac	rs397517245
Gnomad	rs397517245
Varsome	rs397517245
LitVar	rs397517245
Map	rs397517245
PheGenI	rs397517245
Biobank	rs397517245
1000 genomes	rs397517245
hgdp	rs397517245
ensembl	rs397517245
geneview	rs397517245
scholar	rs397517245
google	rs397517245
pharmgkb	rs397517245
gwascentral	rs397517245
openSNP	rs397517245
23andMe	rs397517245
SNPshot	rs397517245
SNPdbe	rs397517245
MSV3d	rs397517245
GWAS Ctlg	rs397517245

Max Magnitude

0

ClinVar
Risk	rs397517245(A;A)
Alt	rs397517245(A;A)
Reference	Rs397517245(-;-)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75834537dupA
CLNSRC	ClinVar
CLNACC	RCV000038836.2,