rs193922712

Orientation

plus

Stabilized

plus

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

Make rs193922712(A;G)

Make rs193922712(G;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

31821560

Gene

MYLK2

is a	snp
is	mentioned by
dbSNP	rs193922712
dbSNP (classic)	rs193922712
ClinGen	rs193922712
ebi	rs193922712
HLI	rs193922712
Exac	rs193922712
Gnomad	rs193922712
Varsome	rs193922712
LitVar	rs193922712
Map	rs193922712
PheGenI	rs193922712
Biobank	rs193922712
1000 genomes	rs193922712
hgdp	rs193922712
ensembl	rs193922712
geneview	rs193922712
scholar	rs193922712
google	rs193922712
pharmgkb	rs193922712
gwascentral	rs193922712
openSNP	rs193922712
23andMe	rs193922712
SNPshot	rs193922712
SNPdbe	rs193922712
MSV3d	rs193922712
GWAS Ctlg	rs193922712

Max Magnitude

0

ClinVar
Risk	rs193922712(G;G)
Alt	rs193922712(G;G)
Reference	Rs193922712(A;A)
Significance	Probable-Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	MYLK2
CLNDBN	Cardiomyopathy
Reversed	0
HGVS	NC_000020.10:g.30409363A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030332.1,