rs397516482

Orientation

minus

Stabilized

minus

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

Make rs397516482(A;T)

Make rs397516482(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201361286

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516482
dbSNP (classic)	rs397516482
ClinGen	rs397516482
ebi	rs397516482
HLI	rs397516482
Exac	rs397516482
Gnomad	rs397516482
Varsome	rs397516482
LitVar	rs397516482
Map	rs397516482
PheGenI	rs397516482
Biobank	rs397516482
1000 genomes	rs397516482
hgdp	rs397516482
ensembl	rs397516482
geneview	rs397516482
scholar	rs397516482
google	rs397516482
pharmgkb	rs397516482
gwascentral	rs397516482
openSNP	rs397516482
23andMe	rs397516482
SNPshot	rs397516482
SNPdbe	rs397516482
MSV3d	rs397516482
GWAS Ctlg	rs397516482

Max Magnitude

0

ClinVar
Risk	rs397516482(T;T)
Alt	rs397516482(T;T)
Reference	Rs397516482(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	TNNT2
CLNDBN	not specified
Reversed	1
HGVS	NC_000001.10:g.201330414T>A
CLNSRC
CLNACC	RCV000036618.3,