rs397516450

Orientation

minus

Stabilized

minus

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

Make rs397516450(A;G)

Make rs397516450(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201365656

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516450
dbSNP (classic)	rs397516450
ClinGen	rs397516450
ebi	rs397516450
HLI	rs397516450
Exac	rs397516450
Gnomad	rs397516450
Varsome	rs397516450
LitVar	rs397516450
Map	rs397516450
PheGenI	rs397516450
Biobank	rs397516450
1000 genomes	rs397516450
hgdp	rs397516450
ensembl	rs397516450
geneview	rs397516450
scholar	rs397516450
google	rs397516450
pharmgkb	rs397516450
gwascentral	rs397516450
openSNP	rs397516450
23andMe	rs397516450
SNPshot	rs397516450
SNPdbe	rs397516450
MSV3d	rs397516450
GWAS Ctlg	rs397516450

Max Magnitude

0

ClinVar
Risk	rs397516450(G;G)
Alt	rs397516450(G;G)
Reference	Rs397516450(A;A)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TNNT2
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000001.10:g.201334784T>C
CLNSRC	ClinVar
CLNACC	RCV000036562.2,