rs730880821

Orientation

minus

Stabilized

minus

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

Make rs730880821(A;A)

Make rs730880821(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23415024

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880821
dbSNP (classic)	rs730880821
ClinGen	rs730880821
ebi	rs730880821
HLI	rs730880821
Exac	rs730880821
Gnomad	rs730880821
Varsome	rs730880821
LitVar	rs730880821
Map	rs730880821
PheGenI	rs730880821
Biobank	rs730880821
1000 genomes	rs730880821
hgdp	rs730880821
ensembl	rs730880821
geneview	rs730880821
scholar	rs730880821
google	rs730880821
pharmgkb	rs730880821
gwascentral	rs730880821
openSNP	rs730880821
23andMe	rs730880821
SNPshot	rs730880821
SNPdbe	rs730880821
MSV3d	rs730880821
GWAS Ctlg	rs730880821

Max Magnitude

0

ClinVar
Risk	rs730880821(A;A)
Alt	rs730880821(A;A)
Reference	Rs730880821(G;G)
Significance	Probable-Pathogenic
Disease	not provided Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7 MHRT
CLNDBN	not provided Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23884233C>T
CLNSRC
CLNACC	RCV000158706.2, RCV000469554.1,