rs730881121

Orientation

minus

Stabilized

minus

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

Make rs730881121(C;T)

Make rs730881121(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201365635

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs730881121
dbSNP (classic)	rs730881121
ClinGen	rs730881121
ebi	rs730881121
HLI	rs730881121
Exac	rs730881121
Gnomad	rs730881121
Varsome	rs730881121
LitVar	rs730881121
Map	rs730881121
PheGenI	rs730881121
Biobank	rs730881121
1000 genomes	rs730881121
hgdp	rs730881121
ensembl	rs730881121
geneview	rs730881121
scholar	rs730881121
google	rs730881121
pharmgkb	rs730881121
gwascentral	rs730881121
openSNP	rs730881121
23andMe	rs730881121
SNPshot	rs730881121
SNPdbe	rs730881121
MSV3d	rs730881121
GWAS Ctlg	rs730881121

Max Magnitude

0

ClinVar
Risk	rs730881121(T;T)
Alt	rs730881121(T;T)
Reference	Rs730881121(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TNNT2
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.201334763G>A
CLNSRC
CLNACC	RCV000159336.1,