rs587776700

Orientation

plus

Stabilized

plus

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

Make rs587776700(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

47347030

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs587776700
dbSNP (classic)	rs587776700
ClinGen	rs587776700
ebi	rs587776700
HLI	rs587776700
Exac	rs587776700
Gnomad	rs587776700
Varsome	rs587776700
LitVar	rs587776700
Map	rs587776700
PheGenI	rs587776700
Biobank	rs587776700
1000 genomes	rs587776700
hgdp	rs587776700
ensembl	rs587776700
geneview	rs587776700
scholar	rs587776700
google	rs587776700
pharmgkb	rs587776700
gwascentral	rs587776700
openSNP	rs587776700
23andMe	rs587776700
SNPshot	rs587776700
SNPdbe	rs587776700
MSV3d	rs587776700
GWAS Ctlg	rs587776700

Max Magnitude

6.2

ClinVar
Risk	rs587776700(G;G) rs587776700(T;T)
Alt	rs587776700(G;G) rs587776700(T;T)
Reference	Rs587776700(C;C)
Significance	Pathogenic
Disease	Familial hypertrophic cardiomyopathy 4 not provided
Variation	info
Gene	MYBPC3
CLNDBN	Familial hypertrophic cardiomyopathy 4 not provided
Reversed	0
HGVS	NC_000011.9:g.47368581C>G; NC_000011.9:g.47368581C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009150.4, RCV000158319.2, RCV000358520.2,