rs779637525

Orientation

plus

Stabilized

plus

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

Make rs779637525(G;T)

Make rs779637525(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

31826918

Gene

MYLK2

is a	snp
is	mentioned by
dbSNP	rs779637525
dbSNP (classic)	rs779637525
ClinGen	rs779637525
ebi	rs779637525
HLI	rs779637525
Exac	rs779637525
Gnomad	rs779637525
Varsome	rs779637525
LitVar	rs779637525
Map	rs779637525
PheGenI	rs779637525
Biobank	rs779637525
1000 genomes	rs779637525
hgdp	rs779637525
ensembl	rs779637525
geneview	rs779637525
scholar	rs779637525
google	rs779637525
pharmgkb	rs779637525
gwascentral	rs779637525
openSNP	rs779637525
23andMe	rs779637525
SNPshot	rs779637525
SNPdbe	rs779637525
MSV3d	rs779637525
GWAS Ctlg	rs779637525

Max Magnitude

0

ClinVar
Risk	rs779637525(T;T)
Alt	rs779637525(T;T)
Reference	Rs779637525(G;G)
Significance	Pathogenic
Disease	not provided Familial hypertrophic cardiomyopathy 1
Variation	info
Gene	MYLK2
CLNDBN	not provided Familial hypertrophic cardiomyopathy 1
Reversed	0
HGVS	NC_000020.10:g.30414721G>T
CLNSRC
CLNACC	RCV000183563.1, RCV000459516.1,