rs730880664

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;C)	6.2	Familial Hypertrophic Cardiomyopathy
(C;C)	0	common in clinvar

Make rs730880664(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

47351294

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs730880664
dbSNP (classic)	rs730880664
ClinGen	rs730880664
ebi	rs730880664
HLI	rs730880664
Exac	rs730880664
Gnomad	rs730880664
Varsome	rs730880664
LitVar	rs730880664
Map	rs730880664
PheGenI	rs730880664
Biobank	rs730880664
1000 genomes	rs730880664
hgdp	rs730880664
ensembl	rs730880664
geneview	rs730880664
scholar	rs730880664
google	rs730880664
pharmgkb	rs730880664
gwascentral	rs730880664
openSNP	rs730880664
23andMe	rs730880664
SNPshot	rs730880664
SNPdbe	rs730880664
MSV3d	rs730880664
GWAS Ctlg	rs730880664

Max Magnitude

6.2

ClinVar
Risk	rs730880664(-;-)
Alt	rs730880664(-;-)
Reference	Rs730880664(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYBPC3
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.47372845delG
CLNSRC
CLNACC	RCV000158386.2,