rs876657705

Orientation

minus

Stabilized

minus

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

Make rs876657705(-;-)

Make rs876657705(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

47335158

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs876657705
dbSNP (classic)	rs876657705
ClinGen	rs876657705
ebi	rs876657705
HLI	rs876657705
Exac	rs876657705
Gnomad	rs876657705
Varsome	rs876657705
LitVar	rs876657705
Map	rs876657705
PheGenI	rs876657705
Biobank	rs876657705
1000 genomes	rs876657705
hgdp	rs876657705
ensembl	rs876657705
geneview	rs876657705
scholar	rs876657705
google	rs876657705
pharmgkb	rs876657705
gwascentral	rs876657705
openSNP	rs876657705
23andMe	rs876657705
SNPshot	rs876657705
SNPdbe	rs876657705
MSV3d	rs876657705
GWAS Ctlg	rs876657705

Max Magnitude

0

ClinVar
Risk	rs876657705(-;-)
Alt	rs876657705(-;-)
Reference	Rs876657705(T;T)
Significance	Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000011.9:g.47356709delA
CLNSRC
CLNACC	RCV000217959.1,