rs397516459

Orientation

minus

Stabilized

minus

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

Make rs397516459(G;T)

Make rs397516459(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201365281

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516459
dbSNP (classic)	rs397516459
ClinGen	rs397516459
ebi	rs397516459
HLI	rs397516459
Exac	rs397516459
Gnomad	rs397516459
Varsome	rs397516459
LitVar	rs397516459
Map	rs397516459
PheGenI	rs397516459
Biobank	rs397516459
1000 genomes	rs397516459
hgdp	rs397516459
ensembl	rs397516459
geneview	rs397516459
scholar	rs397516459
google	rs397516459
pharmgkb	rs397516459
gwascentral	rs397516459
openSNP	rs397516459
23andMe	rs397516459
SNPshot	rs397516459
SNPdbe	rs397516459
MSV3d	rs397516459
GWAS Ctlg	rs397516459

Max Magnitude

0

ClinVar
Risk	rs397516459(A;A) rs397516459(T;T)
Alt	rs397516459(A;A) rs397516459(T;T)
Reference	Rs397516459(G;G)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy not specified
Variation	info
Gene	TNNT2
CLNDBN	Primary familial hypertrophic cardiomyopathy not specified
Reversed	1
HGVS	NC_000001.10:g.201334409C>A
CLNSRC	ClinVar
CLNACC	RCV000036578.3, RCV000223847.1,