rs727503242

Orientation

minus

Stabilized

minus

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

Make rs727503242(C;T)

Make rs727503242(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23415047

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs727503242
dbSNP (classic)	rs727503242
ClinGen	rs727503242
ebi	rs727503242
HLI	rs727503242
Exac	rs727503242
Gnomad	rs727503242
Varsome	rs727503242
LitVar	rs727503242
Map	rs727503242
PheGenI	rs727503242
Biobank	rs727503242
1000 genomes	rs727503242
hgdp	rs727503242
ensembl	rs727503242
geneview	rs727503242
scholar	rs727503242
google	rs727503242
pharmgkb	rs727503242
gwascentral	rs727503242
openSNP	rs727503242
23andMe	rs727503242
SNPshot	rs727503242
SNPdbe	rs727503242
MSV3d	rs727503242
GWAS Ctlg	rs727503242

Max Magnitude

0

ClinVar
Risk	rs727503242(G;G) rs727503242(T;T)
Alt	rs727503242(G;G) rs727503242(T;T)
Reference	Rs727503242(C;C)
Significance	Pathogenic
Disease	not specified Hypertrophic cardiomyopathy not provided
Variation	info
Gene	MYH7 MHRT
CLNDBN	not specified Hypertrophic cardiomyopathy not provided
Reversed	1
HGVS	NC_000014.8:g.23884256G>A; NC_000014.8:g.23884256G>C
CLNSRC
CLNACC	RCV000151235.3, RCV000459205.1, RCV000158705.2,