rs730880635

Orientation

minus

Stabilized

minus

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

Make rs730880635(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

47343595

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs730880635
dbSNP (classic)	rs730880635
ClinGen	rs730880635
ebi	rs730880635
HLI	rs730880635
Exac	rs730880635
Gnomad	rs730880635
Varsome	rs730880635
LitVar	rs730880635
Map	rs730880635
PheGenI	rs730880635
Biobank	rs730880635
1000 genomes	rs730880635
hgdp	rs730880635
ensembl	rs730880635
geneview	rs730880635
scholar	rs730880635
google	rs730880635
pharmgkb	rs730880635
gwascentral	rs730880635
openSNP	rs730880635
23andMe	rs730880635
SNPshot	rs730880635
SNPdbe	rs730880635
MSV3d	rs730880635
GWAS Ctlg	rs730880635

Max Magnitude

6.2

ClinVar
Risk	rs730880635(A;A) rs730880635(T;T)
Alt	rs730880635(A;A) rs730880635(T;T)
Reference	Rs730880635(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYBPC3
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.47365146G>A
CLNSRC
CLNACC	RCV000158333.1,