rs397516452

Orientation

minus

Stabilized

minus

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

Make rs397516452(C;C)

Make rs397516452(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201365623

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516452
dbSNP (classic)	rs397516452
ClinGen	rs397516452
ebi	rs397516452
HLI	rs397516452
Exac	rs397516452
Gnomad	rs397516452
Varsome	rs397516452
LitVar	rs397516452
Map	rs397516452
PheGenI	rs397516452
Biobank	rs397516452
1000 genomes	rs397516452
hgdp	rs397516452
ensembl	rs397516452
geneview	rs397516452
scholar	rs397516452
google	rs397516452
pharmgkb	rs397516452
gwascentral	rs397516452
openSNP	rs397516452
23andMe	rs397516452
SNPshot	rs397516452
SNPdbe	rs397516452
MSV3d	rs397516452
GWAS Ctlg	rs397516452

Max Magnitude

0

ClinVar
Risk	rs397516452(C;C)
Alt	rs397516452(C;C)
Reference	Rs397516452(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided Cardiovascular phenotype
Variation	info
Gene	TNNT2
CLNDBN	not specified not provided Cardiovascular phenotype
Reversed	1
HGVS	NC_000001.10:g.201334751C>G
CLNSRC
CLNACC	RCV000036568.3, RCV000159277.2, RCV000244818.1,