rs794729067

Orientation

plus

Stabilized

plus

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

Make rs794729067(-;-)

Make rs794729067(-;TG)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

31826887

Gene

MYLK2

is a	snp
is	mentioned by
dbSNP	rs794729067
dbSNP (classic)	rs794729067
ClinGen	rs794729067
ebi	rs794729067
HLI	rs794729067
Exac	rs794729067
Gnomad	rs794729067
Varsome	rs794729067
LitVar	rs794729067
Map	rs794729067
PheGenI	rs794729067
Biobank	rs794729067
1000 genomes	rs794729067
hgdp	rs794729067
ensembl	rs794729067
geneview	rs794729067
scholar	rs794729067
google	rs794729067
pharmgkb	rs794729067
gwascentral	rs794729067
openSNP	rs794729067
23andMe	rs794729067
SNPshot	rs794729067
SNPdbe	rs794729067
MSV3d	rs794729067
GWAS Ctlg	rs794729067

Max Magnitude

0

ClinVar
Risk	rs794729067(-;-)
Alt	rs794729067(-;-)
Reference	Rs794729067(TG;TG)
Significance	Probable-Pathogenic
Disease	Cardiomyopathy not provided
Variation	info
Gene	MYLK2
CLNDBN	Cardiomyopathy not provided
Reversed	0
HGVS	NC_000020.10:g.30414690_30414691delTG
CLNSRC
CLNACC	RCV000183562.1, RCV000481664.1,