rs876657703

Orientation

minus

Stabilized

minus

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

Make rs876657703(-;G)

Make rs876657703(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

47342842

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs876657703
dbSNP (classic)	rs876657703
ClinGen	rs876657703
ebi	rs876657703
HLI	rs876657703
Exac	rs876657703
Gnomad	rs876657703
Varsome	rs876657703
LitVar	rs876657703
Map	rs876657703
PheGenI	rs876657703
Biobank	rs876657703
1000 genomes	rs876657703
hgdp	rs876657703
ensembl	rs876657703
geneview	rs876657703
scholar	rs876657703
google	rs876657703
pharmgkb	rs876657703
gwascentral	rs876657703
openSNP	rs876657703
23andMe	rs876657703
SNPshot	rs876657703
SNPdbe	rs876657703
MSV3d	rs876657703
GWAS Ctlg	rs876657703

Max Magnitude

0

ClinVar
Risk	rs876657703(G;G)
Alt	rs876657703(G;G)
Reference	Rs876657703(-;-)
Significance	Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000011.9:g.47364394dupC
CLNSRC
CLNACC	RCV000222228.1,