rs397516344

Orientation

minus

Stabilized

minus

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

Make rs397516344(C;T)

Make rs397516344(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

55154806

Gene

TNNI3

is a	snp
is	mentioned by
dbSNP	rs397516344
dbSNP (classic)	rs397516344
ClinGen	rs397516344
ebi	rs397516344
HLI	rs397516344
Exac	rs397516344
Gnomad	rs397516344
Varsome	rs397516344
LitVar	rs397516344
Map	rs397516344
PheGenI	rs397516344
Biobank	rs397516344
1000 genomes	rs397516344
hgdp	rs397516344
ensembl	rs397516344
geneview	rs397516344
scholar	rs397516344
google	rs397516344
pharmgkb	rs397516344
gwascentral	rs397516344
openSNP	rs397516344
23andMe	rs397516344
SNPshot	rs397516344
SNPdbe	rs397516344
MSV3d	rs397516344
GWAS Ctlg	rs397516344

Max Magnitude

0

ClinVar
Risk	rs397516344(G;G) rs397516344(T;T)
Alt	rs397516344(G;G) rs397516344(T;T)
Reference	Rs397516344(C;C)
Significance	Probable-Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	TNNI3
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000019.9:g.55666174G>A; NC_000019.9:g.55666174G>C
CLNSRC	ClinVar
CLNACC	RCV000036283.3, RCV000198680.1,