rs730881102

Orientation

minus

Stabilized

minus

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

Make rs730881102(A;A)

Make rs730881102(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201364314

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs730881102
dbSNP (classic)	rs730881102
ClinGen	rs730881102
ebi	rs730881102
HLI	rs730881102
Exac	rs730881102
Gnomad	rs730881102
Varsome	rs730881102
LitVar	rs730881102
Map	rs730881102
PheGenI	rs730881102
Biobank	rs730881102
1000 genomes	rs730881102
hgdp	rs730881102
ensembl	rs730881102
geneview	rs730881102
scholar	rs730881102
google	rs730881102
pharmgkb	rs730881102
gwascentral	rs730881102
openSNP	rs730881102
23andMe	rs730881102
SNPshot	rs730881102
SNPdbe	rs730881102
MSV3d	rs730881102
GWAS Ctlg	rs730881102

Max Magnitude

0

ClinVar
Risk	rs730881102(A;A)
Alt	rs730881102(A;A)
Reference	Rs730881102(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNT2
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.201333442C>T
CLNSRC
CLNACC	RCV000159298.2,