rs397516464

Orientation

minus

Stabilized

minus

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

Make rs397516464(A;A)

Make rs397516464(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201364365

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516464
dbSNP (classic)	rs397516464
ClinGen	rs397516464
ebi	rs397516464
HLI	rs397516464
Exac	rs397516464
Gnomad	rs397516464
Varsome	rs397516464
LitVar	rs397516464
Map	rs397516464
PheGenI	rs397516464
Biobank	rs397516464
1000 genomes	rs397516464
hgdp	rs397516464
ensembl	rs397516464
geneview	rs397516464
scholar	rs397516464
google	rs397516464
pharmgkb	rs397516464
gwascentral	rs397516464
openSNP	rs397516464
23andMe	rs397516464
SNPshot	rs397516464
SNPdbe	rs397516464
MSV3d	rs397516464
GWAS Ctlg	rs397516464

Max Magnitude

0

ClinVar
Risk	rs397516464(A;A) rs397516464(C;C)
Alt	rs397516464(A;A) rs397516464(C;C)
Reference	Rs397516464(G;G)
Significance	Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TNNT2
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000001.10:g.201333493C>G; NC_000001.10:g.201333493C>T
CLNSRC	ClinVar
CLNACC	RCV000036586.2, RCV000036585.3,