rs145532615

Orientation

plus

Stabilized

plus

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

Make rs145532615(A;G)

Make rs145532615(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23423701

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs145532615
dbSNP (classic)	rs145532615
ClinGen	rs145532615
ebi	rs145532615
HLI	rs145532615
Exac	rs145532615
Gnomad	rs145532615
Varsome	rs145532615
LitVar	rs145532615
Map	rs145532615
PheGenI	rs145532615
Biobank	rs145532615
1000 genomes	rs145532615
hgdp	rs145532615
ensembl	rs145532615
geneview	rs145532615
scholar	rs145532615
google	rs145532615
pharmgkb	rs145532615
gwascentral	rs145532615
openSNP	rs145532615
23andMe	rs145532615
SNPshot	rs145532615
SNPdbe	rs145532615
MSV3d	rs145532615
GWAS Ctlg	rs145532615

Max Magnitude

0

ClinVar
Risk	rs145532615(G;G)
Alt	rs145532615(G;G)
Reference	Rs145532615(A;A)
Significance	Other
Disease	not specified Increased left ventricular wall thickness Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy Cardiovascular phenotype Scapuloperoneal myopathy Left ventricular noncompaction cardiomyopathy Laing distal myopathy Dilated Cardiomyopathy Myosin storage myopathy
Variation	info
Gene	MYH7
CLNDBN	not specified Increased left ventricular wall thickness Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy Cardiovascular phenotype Scapuloperoneal myopathy Left ventricular noncompaction cardiomyopathy Laing distal myopathy Dilated Cardiomyopathy, Dominant Myosin storage myopathy
Reversed	0
HGVS	NC_000014.8:g.23892910A>G
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000035834.5, RCV000148698.2, RCV000168882.2, RCV000199809.4, RCV000247539.1, RCV000279750.1, RCV000292823.1, RCV000334844.1, RCV000352353.1, RCV000401402.1,