rs149576470

Orientation

plus

Stabilized

plus

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

Make rs149576470(A;A)

Make rs149576470(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23424863

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs149576470
dbSNP (classic)	rs149576470
ClinGen	rs149576470
ebi	rs149576470
HLI	rs149576470
Exac	rs149576470
Gnomad	rs149576470
Varsome	rs149576470
LitVar	rs149576470
Map	rs149576470
PheGenI	rs149576470
Biobank	rs149576470
1000 genomes	rs149576470
hgdp	rs149576470
ensembl	rs149576470
geneview	rs149576470
scholar	rs149576470
google	rs149576470
pharmgkb	rs149576470
gwascentral	rs149576470
openSNP	rs149576470
23andMe	rs149576470
SNPshot	rs149576470
SNPdbe	rs149576470
MSV3d	rs149576470
GWAS Ctlg	rs149576470

Max Magnitude

0

ClinVar
Risk	rs149576470(A;A)
Alt	rs149576470(A;A)
Reference	Rs149576470(G;G)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Primary dilated cardiomyopathy Hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000014.8:g.23894072G>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030314.1, RCV000464813.1,