rs730881079

Orientation

minus

Stabilized

minus

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

Make rs730881079(A;G)

Make rs730881079(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

55151913

Gene

TNNI3

is a	snp
is	mentioned by
dbSNP	rs730881079
dbSNP (classic)	rs730881079
ClinGen	rs730881079
ebi	rs730881079
HLI	rs730881079
Exac	rs730881079
Gnomad	rs730881079
Varsome	rs730881079
LitVar	rs730881079
Map	rs730881079
PheGenI	rs730881079
Biobank	rs730881079
1000 genomes	rs730881079
hgdp	rs730881079
ensembl	rs730881079
geneview	rs730881079
scholar	rs730881079
google	rs730881079
pharmgkb	rs730881079
gwascentral	rs730881079
openSNP	rs730881079
23andMe	rs730881079
SNPshot	rs730881079
SNPdbe	rs730881079
MSV3d	rs730881079
GWAS Ctlg	rs730881079

Max Magnitude

0

ClinVar
Risk	rs730881079(G;G)
Alt	rs730881079(G;G)
Reference	Rs730881079(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNI3
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.55663281T>C
CLNSRC
CLNACC	RCV000159238.2,