rs397515897

Orientation

minus

Stabilized

minus

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

Make rs397515897(C;C)

Make rs397515897(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

47343019

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs397515897
dbSNP (classic)	rs397515897
ClinGen	rs397515897
ebi	rs397515897
HLI	rs397515897
Exac	rs397515897
Gnomad	rs397515897
Varsome	rs397515897
LitVar	rs397515897
Map	rs397515897
PheGenI	rs397515897
Biobank	rs397515897
1000 genomes	rs397515897
hgdp	rs397515897
ensembl	rs397515897
geneview	rs397515897
scholar	rs397515897
google	rs397515897
pharmgkb	rs397515897
gwascentral	rs397515897
openSNP	rs397515897
23andMe	rs397515897
SNPshot	rs397515897
SNPdbe	rs397515897
MSV3d	rs397515897
GWAS Ctlg	rs397515897

Max Magnitude

0

ClinVar
Risk	rs397515897(C;C)
Alt	rs397515897(C;C)
Reference	Rs397515897(T;T)
Significance	Pathogenic
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.47364570A>G
CLNSRC	ClinVar
CLNACC	RCV000035391.2, RCV000158072.1,