rs397516010

Orientation

minus

Stabilized

minus

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

Make rs397516010(G;T)

Make rs397516010(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

47333271

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs397516010
dbSNP (classic)	rs397516010
ClinGen	rs397516010
ebi	rs397516010
HLI	rs397516010
Exac	rs397516010
Gnomad	rs397516010
Varsome	rs397516010
LitVar	rs397516010
Map	rs397516010
PheGenI	rs397516010
Biobank	rs397516010
1000 genomes	rs397516010
hgdp	rs397516010
ensembl	rs397516010
geneview	rs397516010
scholar	rs397516010
google	rs397516010
pharmgkb	rs397516010
gwascentral	rs397516010
openSNP	rs397516010
23andMe	rs397516010
SNPshot	rs397516010
SNPdbe	rs397516010
MSV3d	rs397516010
GWAS Ctlg	rs397516010

Max Magnitude

0

ClinVar
Risk	rs397516010(C;C) rs397516010(T;T)
Alt	rs397516010(C;C) rs397516010(T;T)
Reference	Rs397516010(G;G)
Significance	Other
Disease	Primary familial hypertrophic cardiomyopathy not provided
Variation	info
Gene	MYBPC3
CLNDBN	Primary familial hypertrophic cardiomyopathy not provided
Reversed	1
HGVS	NC_000011.9:g.47354822C>A
CLNSRC	ClinVar
CLNACC	RCV000208092.2, RCV000255392.1,