rs727503513

Orientation

minus

Stabilized

minus

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

Make rs727503513(C;T)

Make rs727503513(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201365292

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs727503513
dbSNP (classic)	rs727503513
ClinGen	rs727503513
ebi	rs727503513
HLI	rs727503513
Exac	rs727503513
Gnomad	rs727503513
Varsome	rs727503513
LitVar	rs727503513
Map	rs727503513
PheGenI	rs727503513
Biobank	rs727503513
1000 genomes	rs727503513
hgdp	rs727503513
ensembl	rs727503513
geneview	rs727503513
scholar	rs727503513
google	rs727503513
pharmgkb	rs727503513
gwascentral	rs727503513
openSNP	rs727503513
23andMe	rs727503513
SNPshot	rs727503513
SNPdbe	rs727503513
MSV3d	rs727503513
GWAS Ctlg	rs727503513

Max Magnitude

0

ClinVar
Risk	rs727503513(T;T)
Alt	rs727503513(T;T)
Reference	Rs727503513(C;C)
Significance	Other
Disease	Familial restrictive cardiomyopathy not provided
Variation	info
Gene	TNNT2
CLNDBN	Familial restrictive cardiomyopathy not provided
Reversed	1
HGVS	NC_000001.10:g.201334420G>A
CLNSRC
CLNACC	RCV000152104.1, RCV000159282.2,