rs397517239

Orientation

plus

Stabilized

plus

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

Make rs397517239(C;T)

Make rs397517239(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

74070743

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs397517239
dbSNP (classic)	rs397517239
ClinGen	rs397517239
ebi	rs397517239
HLI	rs397517239
Exac	rs397517239
Gnomad	rs397517239
Varsome	rs397517239
LitVar	rs397517239
Map	rs397517239
PheGenI	rs397517239
Biobank	rs397517239
1000 genomes	rs397517239
hgdp	rs397517239
ensembl	rs397517239
geneview	rs397517239
scholar	rs397517239
google	rs397517239
pharmgkb	rs397517239
gwascentral	rs397517239
openSNP	rs397517239
23andMe	rs397517239
SNPshot	rs397517239
SNPdbe	rs397517239
MSV3d	rs397517239
GWAS Ctlg	rs397517239

Max Magnitude

0

ClinVar
Risk	rs397517239(T;T)
Alt	rs397517239(T;T)
Reference	Rs397517239(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75830501C>T
CLNSRC	ClinVar
CLNACC	RCV000038823.2,