rs199669878

Orientation

plus

Stabilized

plus

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

Make rs199669878(C;T)

Make rs199669878(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

47332658

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs199669878
dbSNP (classic)	rs199669878
ClinGen	rs199669878
ebi	rs199669878
HLI	rs199669878
Exac	rs199669878
Gnomad	rs199669878
Varsome	rs199669878
LitVar	rs199669878
Map	rs199669878
PheGenI	rs199669878
Biobank	rs199669878
1000 genomes	rs199669878
hgdp	rs199669878
ensembl	rs199669878
geneview	rs199669878
scholar	rs199669878
google	rs199669878
pharmgkb	rs199669878
gwascentral	rs199669878
openSNP	rs199669878
23andMe	rs199669878
SNPshot	rs199669878
SNPdbe	rs199669878
MSV3d	rs199669878
GWAS Ctlg	rs199669878

Max Magnitude

0

ClinVar
Risk	rs199669878(T;T)
Alt	rs199669878(T;T)
Reference	Rs199669878(C;C)
Significance	Probable-non-pathogenic
Disease	not specified not provided Hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	not specified not provided Hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000011.9:g.47354209C>T
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000035594.6, RCV000172003.1, RCV000234600.2,