rs876657706

Orientation

minus

Stabilized

minus

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

Make rs876657706(-;-)

Make rs876657706(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

47332681

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs876657706
dbSNP (classic)	rs876657706
ClinGen	rs876657706
ebi	rs876657706
HLI	rs876657706
Exac	rs876657706
Gnomad	rs876657706
Varsome	rs876657706
LitVar	rs876657706
Map	rs876657706
PheGenI	rs876657706
Biobank	rs876657706
1000 genomes	rs876657706
hgdp	rs876657706
ensembl	rs876657706
geneview	rs876657706
scholar	rs876657706
google	rs876657706
pharmgkb	rs876657706
gwascentral	rs876657706
openSNP	rs876657706
23andMe	rs876657706
SNPshot	rs876657706
SNPdbe	rs876657706
MSV3d	rs876657706
GWAS Ctlg	rs876657706

Max Magnitude

0

ClinVar
Risk	rs876657706(-;-)
Alt	rs876657706(-;-)
Reference	Rs876657706(A;A)
Significance	Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000011.9:g.47354232delT
CLNSRC
CLNACC	RCV000215999.1,