rs730881059

Orientation

minus

Stabilized

minus

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

Make rs730881059(A;A)

Make rs730881059(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

52451771

Gene

TNNC1

is a	snp
is	mentioned by
dbSNP	rs730881059
dbSNP (classic)	rs730881059
ClinGen	rs730881059
ebi	rs730881059
HLI	rs730881059
Exac	rs730881059
Gnomad	rs730881059
Varsome	rs730881059
LitVar	rs730881059
Map	rs730881059
PheGenI	rs730881059
Biobank	rs730881059
1000 genomes	rs730881059
hgdp	rs730881059
ensembl	rs730881059
geneview	rs730881059
scholar	rs730881059
google	rs730881059
pharmgkb	rs730881059
gwascentral	rs730881059
openSNP	rs730881059
23andMe	rs730881059
SNPshot	rs730881059
SNPdbe	rs730881059
MSV3d	rs730881059
GWAS Ctlg	rs730881059

Max Magnitude

0

ClinVar
Risk	rs730881059(A;A)
Alt	rs730881059(A;A)
Reference	Rs730881059(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNC1
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.52485787A>T
CLNSRC
CLNACC	RCV000159196.1,