rs397516469

Orientation

minus

Stabilized

minus

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

Make rs397516469(C;T)

Make rs397516469(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201363391

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516469
dbSNP (classic)	rs397516469
ClinGen	rs397516469
ebi	rs397516469
HLI	rs397516469
Exac	rs397516469
Gnomad	rs397516469
Varsome	rs397516469
LitVar	rs397516469
Map	rs397516469
PheGenI	rs397516469
Biobank	rs397516469
1000 genomes	rs397516469
hgdp	rs397516469
ensembl	rs397516469
geneview	rs397516469
scholar	rs397516469
google	rs397516469
pharmgkb	rs397516469
gwascentral	rs397516469
openSNP	rs397516469
23andMe	rs397516469
SNPshot	rs397516469
SNPdbe	rs397516469
MSV3d	rs397516469
GWAS Ctlg	rs397516469

Max Magnitude

0

ClinVar
Risk	rs397516469(T;T)
Alt	rs397516469(T;T)
Reference	Rs397516469(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TNNT2
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000001.10:g.201332519G>A
CLNSRC	ClinVar
CLNACC	RCV000036594.2,