rs397516466

Orientation

minus

Stabilized

minus

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

Make rs397516466(A;A)

Make rs397516466(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201364341

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs397516466
dbSNP (classic)	rs397516466
ClinGen	rs397516466
ebi	rs397516466
HLI	rs397516466
Exac	rs397516466
Gnomad	rs397516466
Varsome	rs397516466
LitVar	rs397516466
Map	rs397516466
PheGenI	rs397516466
Biobank	rs397516466
1000 genomes	rs397516466
hgdp	rs397516466
ensembl	rs397516466
geneview	rs397516466
scholar	rs397516466
google	rs397516466
pharmgkb	rs397516466
gwascentral	rs397516466
openSNP	rs397516466
23andMe	rs397516466
SNPshot	rs397516466
SNPdbe	rs397516466
MSV3d	rs397516466
GWAS Ctlg	rs397516466

Max Magnitude

0

ClinVar
Risk	rs397516466(A;A)
Alt	rs397516466(A;A)
Reference	Rs397516466(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	TNNT2
CLNDBN	not specified not provided
Reversed	1
HGVS	NC_000001.10:g.201333469C>T
CLNSRC	ClinVar
CLNACC	RCV000036590.3, RCV000159295.3,