rs45525839

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	6.2	Dilated cardiomyopathy

Make rs45525839(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201364357

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs45525839
dbSNP (classic)	rs45525839
ClinGen	rs45525839
ebi	rs45525839
HLI	rs45525839
Exac	rs45525839
Gnomad	rs45525839
Varsome	rs45525839
LitVar	rs45525839
Map	rs45525839
PheGenI	rs45525839
Biobank	rs45525839
1000 genomes	rs45525839
hgdp	rs45525839
ensembl	rs45525839
geneview	rs45525839
scholar	rs45525839
google	rs45525839
pharmgkb	rs45525839
gwascentral	rs45525839
openSNP	rs45525839
23andMe	rs45525839
SNPshot	rs45525839
SNPdbe	rs45525839
MSV3d	rs45525839
GWAS Ctlg	rs45525839

Max Magnitude

6.2

ClinVar
Risk	rs45525839(A;A) rs45525839(G;G) rs45525839(T;T)
Alt	rs45525839(A;A) rs45525839(G;G) rs45525839(T;T)
Reference	Rs45525839(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TNNT2
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000001.10:g.201333485G>A; NC_000001.10:g.201333485G>C
CLNSRC	ClinVar
CLNACC	RCV000172139.2, RCV000036587.2,