rs45466197

Orientation

minus

Stabilized

minus

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

Make rs45466197(G;T)

Make rs45466197(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201361327

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs45466197
dbSNP (classic)	rs45466197
ClinGen	rs45466197
ebi	rs45466197
HLI	rs45466197
Exac	rs45466197
Gnomad	rs45466197
Varsome	rs45466197
LitVar	rs45466197
Map	rs45466197
PheGenI	rs45466197
Biobank	rs45466197
1000 genomes	rs45466197
hgdp	rs45466197
ensembl	rs45466197
geneview	rs45466197
scholar	rs45466197
google	rs45466197
pharmgkb	rs45466197
gwascentral	rs45466197
openSNP	rs45466197
23andMe	rs45466197
SNPshot	rs45466197
SNPdbe	rs45466197
MSV3d	rs45466197
GWAS Ctlg	rs45466197

Max Magnitude

0

ClinVar
Risk	rs45466197(T;T)
Alt	rs45466197(T;T)
Reference	Rs45466197(G;G)
Significance	Other
Disease	not specified Primary familial hypertrophic cardiomyopathy not provided Left ventricular noncompaction 6 Familial hypertrophic cardiomyopathy 2
Variation	info
Gene	TNNT2
CLNDBN	not specified Primary familial hypertrophic cardiomyopathy not provided Left ventricular noncompaction 6 Familial hypertrophic cardiomyopathy 2
Reversed	1
HGVS	NC_000001.10:g.201330455C>A
CLNSRC
CLNACC	RCV000036615.3, RCV000148901.1, RCV000225695.1, RCV000415651.1, RCV000415695.1,