rs397516465

Orientation

minus

Stabilized

minus

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

Make rs397516465(C;T)

Make rs397516465(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201364342

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516465
dbSNP (classic)	rs397516465
ClinGen	rs397516465
ebi	rs397516465
HLI	rs397516465
Exac	rs397516465
Gnomad	rs397516465
Varsome	rs397516465
LitVar	rs397516465
Map	rs397516465
PheGenI	rs397516465
Biobank	rs397516465
1000 genomes	rs397516465
hgdp	rs397516465
ensembl	rs397516465
geneview	rs397516465
scholar	rs397516465
google	rs397516465
pharmgkb	rs397516465
gwascentral	rs397516465
openSNP	rs397516465
23andMe	rs397516465
SNPshot	rs397516465
SNPdbe	rs397516465
MSV3d	rs397516465
GWAS Ctlg	rs397516465

Max Magnitude

0

ClinVar
Risk	rs397516465(T;T)
Alt	rs397516465(T;T)
Reference	Rs397516465(C;C)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	TNNT2
CLNDBN	not specified not provided
Reversed	1
HGVS	NC_000001.10:g.201333470G>A; NC_000001.10:g.201333470G>T
CLNSRC
CLNACC	RCV000036588.3, RCV000493712.1,