rs730881062

Orientation

minus

Stabilized

minus

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

Make rs730881062(A;G)

Make rs730881062(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

52451399

Gene

TNNC1

is a	snp
is	mentioned by
dbSNP	rs730881062
dbSNP (classic)	rs730881062
ClinGen	rs730881062
ebi	rs730881062
HLI	rs730881062
Exac	rs730881062
Gnomad	rs730881062
Varsome	rs730881062
LitVar	rs730881062
Map	rs730881062
PheGenI	rs730881062
Biobank	rs730881062
1000 genomes	rs730881062
hgdp	rs730881062
ensembl	rs730881062
geneview	rs730881062
scholar	rs730881062
google	rs730881062
pharmgkb	rs730881062
gwascentral	rs730881062
openSNP	rs730881062
23andMe	rs730881062
SNPshot	rs730881062
SNPdbe	rs730881062
MSV3d	rs730881062
GWAS Ctlg	rs730881062

Max Magnitude

0

ClinVar
Risk	rs730881062(G;G)
Alt	rs730881062(G;G)
Reference	Rs730881062(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNC1
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.52485415T>C
CLNSRC
CLNACC	RCV000159201.2,