rs587776699

Orientation

plus

Stabilized

plus

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

Make rs587776699(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

47343281

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs587776699
dbSNP (classic)	rs587776699
ClinGen	rs587776699
ebi	rs587776699
HLI	rs587776699
Exac	rs587776699
Gnomad	rs587776699
Varsome	rs587776699
LitVar	rs587776699
Map	rs587776699
PheGenI	rs587776699
Biobank	rs587776699
1000 genomes	rs587776699
hgdp	rs587776699
ensembl	rs587776699
geneview	rs587776699
scholar	rs587776699
google	rs587776699
pharmgkb	rs587776699
gwascentral	rs587776699
openSNP	rs587776699
23andMe	rs587776699
SNPshot	rs587776699
SNPdbe	rs587776699
MSV3d	rs587776699
GWAS Ctlg	rs587776699

Max Magnitude

6.2

ClinVar
Risk	rs587776699(T;T)
Alt	rs587776699(T;T)
Reference	Rs587776699(C;C)
Significance	Other
Disease	Familial hypertrophic cardiomyopathy 4 not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	Familial hypertrophic cardiomyopathy 4 not specified Hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000011.9:g.47364832C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009149.4, RCV000168768.2, RCV000467263.1,