rs397515997

Orientation

minus

Stabilized

minus

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

Make rs397515997(-;-)

Make rs397515997(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

47333707

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs397515997
dbSNP (classic)	rs397515997
ClinGen	rs397515997
ebi	rs397515997
HLI	rs397515997
Exac	rs397515997
Gnomad	rs397515997
Varsome	rs397515997
LitVar	rs397515997
Map	rs397515997
PheGenI	rs397515997
Biobank	rs397515997
1000 genomes	rs397515997
hgdp	rs397515997
ensembl	rs397515997
geneview	rs397515997
scholar	rs397515997
google	rs397515997
pharmgkb	rs397515997
gwascentral	rs397515997
openSNP	rs397515997
23andMe	rs397515997
SNPshot	rs397515997
SNPdbe	rs397515997
MSV3d	rs397515997
GWAS Ctlg	rs397515997

Max Magnitude

0

ClinVar
Risk	rs397515997(-;-)
Alt	rs397515997(-;-)
Reference	Rs397515997(C;C)
Significance	Other
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000011.9:g.47355258delG
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000211813.1,