rs1060505018

Orientation

minus

Stabilized

minus

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

Make rs1060505018(G;T)

Make rs1060505018(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

23424817

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs1060505018
dbSNP (classic)	rs1060505018
ClinGen	rs1060505018
ebi	rs1060505018
HLI	rs1060505018
Exac	rs1060505018
Gnomad	rs1060505018
Varsome	rs1060505018
LitVar	rs1060505018
Map	rs1060505018
PheGenI	rs1060505018
Biobank	rs1060505018
1000 genomes	rs1060505018
hgdp	rs1060505018
ensembl	rs1060505018
geneview	rs1060505018
scholar	rs1060505018
google	rs1060505018
pharmgkb	rs1060505018
gwascentral	rs1060505018
openSNP	rs1060505018
23andMe	rs1060505018
SNPshot	rs1060505018
SNPdbe	rs1060505018
MSV3d	rs1060505018
GWAS Ctlg	rs1060505018

Max Magnitude

0

ClinVar
Risk	rs1060505018(T;T)
Alt	rs1060505018(T;T)
Reference	Rs1060505018(G;G)
Significance	Pathogenic
Disease	Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23894026C>A
CLNSRC
CLNACC	RCV000477668.1,