rs730881103

Orientation

minus

Stabilized

minus

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

Make rs730881103(C;G)

Make rs730881103(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201363394

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs730881103
dbSNP (classic)	rs730881103
ClinGen	rs730881103
ebi	rs730881103
HLI	rs730881103
Exac	rs730881103
Gnomad	rs730881103
Varsome	rs730881103
LitVar	rs730881103
Map	rs730881103
PheGenI	rs730881103
Biobank	rs730881103
1000 genomes	rs730881103
hgdp	rs730881103
ensembl	rs730881103
geneview	rs730881103
scholar	rs730881103
google	rs730881103
pharmgkb	rs730881103
gwascentral	rs730881103
openSNP	rs730881103
23andMe	rs730881103
SNPshot	rs730881103
SNPdbe	rs730881103
MSV3d	rs730881103
GWAS Ctlg	rs730881103

Max Magnitude

0

ClinVar
Risk	rs730881103(G;G) rs730881103(T;T)
Alt	rs730881103(G;G) rs730881103(T;T)
Reference	Rs730881103(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	TNNT2
CLNDBN	not specified
Reversed	1
HGVS	NC_000001.10:g.201332522G>C
CLNSRC
CLNACC	RCV000159300.3,