rs730881113

Orientation

minus

Stabilized

minus

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

Make rs730881113(A;A)

Make rs730881113(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201361274

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs730881113
dbSNP (classic)	rs730881113
ClinGen	rs730881113
ebi	rs730881113
HLI	rs730881113
Exac	rs730881113
Gnomad	rs730881113
Varsome	rs730881113
LitVar	rs730881113
Map	rs730881113
PheGenI	rs730881113
Biobank	rs730881113
1000 genomes	rs730881113
hgdp	rs730881113
ensembl	rs730881113
geneview	rs730881113
scholar	rs730881113
google	rs730881113
pharmgkb	rs730881113
gwascentral	rs730881113
openSNP	rs730881113
23andMe	rs730881113
SNPshot	rs730881113
SNPdbe	rs730881113
MSV3d	rs730881113
GWAS Ctlg	rs730881113

Max Magnitude

0

ClinVar
Risk	rs730881113(A;A) rs730881113(C;C)
Alt	rs730881113(A;A) rs730881113(C;C)
Reference	Rs730881113(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNT2
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.201330402C>T
CLNSRC
CLNACC	RCV000159318.2,