rs397517234

Orientation

plus

Stabilized

plus

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

Make rs397517234(C;T)

Make rs397517234(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

74095751

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs397517234
dbSNP (classic)	rs397517234
ClinGen	rs397517234
ebi	rs397517234
HLI	rs397517234
Exac	rs397517234
Gnomad	rs397517234
Varsome	rs397517234
LitVar	rs397517234
Map	rs397517234
PheGenI	rs397517234
Biobank	rs397517234
1000 genomes	rs397517234
hgdp	rs397517234
ensembl	rs397517234
geneview	rs397517234
scholar	rs397517234
google	rs397517234
pharmgkb	rs397517234
gwascentral	rs397517234
openSNP	rs397517234
23andMe	rs397517234
SNPshot	rs397517234
SNPdbe	rs397517234
MSV3d	rs397517234
GWAS Ctlg	rs397517234

Max Magnitude

0

ClinVar
Risk	rs397517234(T;T)
Alt	rs397517234(T;T)
Reference	Rs397517234(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75855509C>T
CLNSRC	ClinVar
CLNACC	RCV000038802.3,