rs730881065

Orientation

minus

Stabilized

minus

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

Make rs730881065(C;G)

Make rs730881065(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

52452153

Gene

TNNC1

is a	snp
is	mentioned by
dbSNP	rs730881065
dbSNP (classic)	rs730881065
ClinGen	rs730881065
ebi	rs730881065
HLI	rs730881065
Exac	rs730881065
Gnomad	rs730881065
Varsome	rs730881065
LitVar	rs730881065
Map	rs730881065
PheGenI	rs730881065
Biobank	rs730881065
1000 genomes	rs730881065
hgdp	rs730881065
ensembl	rs730881065
geneview	rs730881065
scholar	rs730881065
google	rs730881065
pharmgkb	rs730881065
gwascentral	rs730881065
openSNP	rs730881065
23andMe	rs730881065
SNPshot	rs730881065
SNPdbe	rs730881065
MSV3d	rs730881065
GWAS Ctlg	rs730881065

Max Magnitude

0

ClinVar
Risk	rs730881065(G;G)
Alt	rs730881065(G;G)
Reference	Rs730881065(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNC1
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.52486169G>C
CLNSRC
CLNACC	RCV000159206.1,