rs730881066

Orientation

minus

Stabilized

minus

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

Make rs730881066(A;T)

Make rs730881066(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

55156639

Gene

TNNI3

is a	snp
is	mentioned by
dbSNP	rs730881066
dbSNP (classic)	rs730881066
ClinGen	rs730881066
ebi	rs730881066
HLI	rs730881066
Exac	rs730881066
Gnomad	rs730881066
Varsome	rs730881066
LitVar	rs730881066
Map	rs730881066
PheGenI	rs730881066
Biobank	rs730881066
1000 genomes	rs730881066
hgdp	rs730881066
ensembl	rs730881066
geneview	rs730881066
scholar	rs730881066
google	rs730881066
pharmgkb	rs730881066
gwascentral	rs730881066
openSNP	rs730881066
23andMe	rs730881066
SNPshot	rs730881066
SNPdbe	rs730881066
MSV3d	rs730881066
GWAS Ctlg	rs730881066

Max Magnitude

0

ClinVar
Risk	rs730881066(T;T)
Alt	rs730881066(T;T)
Reference	Rs730881066(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNNI3
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.55668007T>A
CLNSRC
CLNACC	RCV000159209.1,