rs730881098

Orientation

minus

Stabilized

minus

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

Make rs730881098(G;G)

Make rs730881098(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201365613

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs730881098
dbSNP (classic)	rs730881098
ClinGen	rs730881098
ebi	rs730881098
HLI	rs730881098
Exac	rs730881098
Gnomad	rs730881098
Varsome	rs730881098
LitVar	rs730881098
Map	rs730881098
PheGenI	rs730881098
Biobank	rs730881098
1000 genomes	rs730881098
hgdp	rs730881098
ensembl	rs730881098
geneview	rs730881098
scholar	rs730881098
google	rs730881098
pharmgkb	rs730881098
gwascentral	rs730881098
openSNP	rs730881098
23andMe	rs730881098
SNPshot	rs730881098
SNPdbe	rs730881098
MSV3d	rs730881098
GWAS Ctlg	rs730881098

Max Magnitude

0

ClinVar
Risk	rs730881098(G;G)
Alt	rs730881098(G;G)
Reference	Rs730881098(T;T)
Significance	Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	TNNT2
CLNDBN	Cardiomyopathy
Reversed	1
HGVS	NC_000001.10:g.201334741A>C
CLNSRC
CLNACC	RCV000159279.1,