rs730881058

Orientation

minus

Stabilized

minus

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

Make rs730881058(A;A)

Make rs730881058(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

52451799

Gene

TNNC1

is a	snp
is	mentioned by
dbSNP	rs730881058
dbSNP (classic)	rs730881058
ClinGen	rs730881058
ebi	rs730881058
HLI	rs730881058
Exac	rs730881058
Gnomad	rs730881058
Varsome	rs730881058
LitVar	rs730881058
Map	rs730881058
PheGenI	rs730881058
Biobank	rs730881058
1000 genomes	rs730881058
hgdp	rs730881058
ensembl	rs730881058
geneview	rs730881058
scholar	rs730881058
google	rs730881058
pharmgkb	rs730881058
gwascentral	rs730881058
openSNP	rs730881058
23andMe	rs730881058
SNPshot	rs730881058
SNPdbe	rs730881058
MSV3d	rs730881058
GWAS Ctlg	rs730881058

Max Magnitude

0

ClinVar
Risk	rs730881058(A;A)
Alt	rs730881058(A;A)
Reference	Rs730881058(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNC1
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.52485815C>T
CLNSRC
CLNACC	RCV000159195.1,