rs727504381

Orientation

plus

Stabilized

plus

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

Make rs727504381(C;T)

Make rs727504381(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

74097222

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs727504381
dbSNP (classic)	rs727504381
ClinGen	rs727504381
ebi	rs727504381
HLI	rs727504381
Exac	rs727504381
Gnomad	rs727504381
Varsome	rs727504381
LitVar	rs727504381
Map	rs727504381
PheGenI	rs727504381
Biobank	rs727504381
1000 genomes	rs727504381
hgdp	rs727504381
ensembl	rs727504381
geneview	rs727504381
scholar	rs727504381
google	rs727504381
pharmgkb	rs727504381
gwascentral	rs727504381
openSNP	rs727504381
23andMe	rs727504381
SNPshot	rs727504381
SNPdbe	rs727504381
MSV3d	rs727504381
GWAS Ctlg	rs727504381

Max Magnitude

0

ClinVar
Risk	rs727504381(T;T)
Alt	rs727504381(T;T)
Reference	Rs727504381(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75856980C>T
CLNSRC
CLNACC	RCV000154540.1,