rs397516352

Orientation

minus

Stabilized

minus

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

Make rs397516352(C;C)

Make rs397516352(C;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

55154115

Gene

TNNI3

is a	snp
is	mentioned by
dbSNP	rs397516352
dbSNP (classic)	rs397516352
ClinGen	rs397516352
ebi	rs397516352
HLI	rs397516352
Exac	rs397516352
Gnomad	rs397516352
Varsome	rs397516352
LitVar	rs397516352
Map	rs397516352
PheGenI	rs397516352
Biobank	rs397516352
1000 genomes	rs397516352
hgdp	rs397516352
ensembl	rs397516352
geneview	rs397516352
scholar	rs397516352
google	rs397516352
pharmgkb	rs397516352
gwascentral	rs397516352
openSNP	rs397516352
23andMe	rs397516352
SNPshot	rs397516352
SNPdbe	rs397516352
MSV3d	rs397516352
GWAS Ctlg	rs397516352

Max Magnitude

0

ClinVar
Risk	rs397516352(C;C)
Alt	rs397516352(C;C)
Reference	Rs397516352(T;T)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TNNI3
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000019.9:g.55665483A>G
CLNSRC	ClinVar
CLNACC	RCV000036298.2,