rs1060501436

Orientation

minus

Stabilized

minus

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

Make rs1060501436(C;C)

Make rs1060501436(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

23424815

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs1060501436
dbSNP (classic)	rs1060501436
ClinGen	rs1060501436
ebi	rs1060501436
HLI	rs1060501436
Exac	rs1060501436
Gnomad	rs1060501436
Varsome	rs1060501436
LitVar	rs1060501436
Map	rs1060501436
PheGenI	rs1060501436
Biobank	rs1060501436
1000 genomes	rs1060501436
hgdp	rs1060501436
ensembl	rs1060501436
geneview	rs1060501436
scholar	rs1060501436
google	rs1060501436
pharmgkb	rs1060501436
gwascentral	rs1060501436
openSNP	rs1060501436
23andMe	rs1060501436
SNPshot	rs1060501436
SNPdbe	rs1060501436
MSV3d	rs1060501436
GWAS Ctlg	rs1060501436

Max Magnitude

0

ClinVar
Risk	rs1060501436(C;C)
Alt	rs1060501436(C;C)
Reference	Rs1060501436(T;T)
Significance	Probable-Pathogenic
Disease	Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23894024A>G
CLNSRC
CLNACC	RCV000472927.1,