rs1060501432

Orientation

minus

Stabilized

minus

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

Make rs1060501432(G;G)

Make rs1060501432(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

23425973

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs1060501432
dbSNP (classic)	rs1060501432
ClinGen	rs1060501432
ebi	rs1060501432
HLI	rs1060501432
Exac	rs1060501432
Gnomad	rs1060501432
Varsome	rs1060501432
LitVar	rs1060501432
Map	rs1060501432
PheGenI	rs1060501432
Biobank	rs1060501432
1000 genomes	rs1060501432
hgdp	rs1060501432
ensembl	rs1060501432
geneview	rs1060501432
scholar	rs1060501432
google	rs1060501432
pharmgkb	rs1060501432
gwascentral	rs1060501432
openSNP	rs1060501432
23andMe	rs1060501432
SNPshot	rs1060501432
SNPdbe	rs1060501432
MSV3d	rs1060501432
GWAS Ctlg	rs1060501432

Max Magnitude

0

ClinVar
Risk	rs1060501432(G;G)
Alt	rs1060501432(G;G)
Reference	Rs1060501432(T;T)
Significance	Probable-Pathogenic
Disease	Hypertrophic cardiomyopathy not provided
Variation	info
Gene	MYH7
CLNDBN	Hypertrophic cardiomyopathy not provided
Reversed	1
HGVS	NC_000014.8:g.23895182A>C
CLNSRC
CLNACC	RCV000473139.1, RCV000486340.1,