rs74315380

Orientation

minus

Stabilized

minus

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

Make rs74315380(C;T)

Make rs74315380(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201364366

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs74315380
dbSNP (classic)	rs74315380
ClinGen	rs74315380
ebi	rs74315380
HLI	rs74315380
Exac	rs74315380
Gnomad	rs74315380
Varsome	rs74315380
LitVar	rs74315380
Map	rs74315380
PheGenI	rs74315380
Biobank	rs74315380
1000 genomes	rs74315380
hgdp	rs74315380
ensembl	rs74315380
geneview	rs74315380
scholar	rs74315380
google	rs74315380
pharmgkb	rs74315380
gwascentral	rs74315380
openSNP	rs74315380
23andMe	rs74315380
SNPshot	rs74315380
SNPdbe	rs74315380
MSV3d	rs74315380
GWAS Ctlg	rs74315380

Max Magnitude

0

OMIM	191045
Desc
Variant	0007
Related	also

OMIM	191045
Desc
Variant	0008
Related	also

ClinVar
Risk	rs74315380(G;G) rs74315380(T;T)
Alt	rs74315380(G;G) rs74315380(T;T)
Reference	Rs74315380(C;C)
Significance	Other
Disease	Left ventricular noncompaction 6 Primary dilated cardiomyopathy not provided
Variation	info
Gene	TNNT2
CLNDBN	Left ventricular noncompaction 6 Primary dilated cardiomyopathy not provided
Reversed	1
HGVS	NC_000001.10:g.201333494G>A; NC_000001.10:g.201333494G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013226.27, RCV000030567.1, RCV000159291.2, RCV000441620.1,