rs368861241

Orientation

plus

Stabilized

plus

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

Make rs368861241(A;A)

Make rs368861241(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

55154095

Gene

TNNI3

is a	snp
is	mentioned by
dbSNP	rs368861241
dbSNP (classic)	rs368861241
ClinGen	rs368861241
ebi	rs368861241
HLI	rs368861241
Exac	rs368861241
Gnomad	rs368861241
Varsome	rs368861241
LitVar	rs368861241
Map	rs368861241
PheGenI	rs368861241
Biobank	rs368861241
1000 genomes	rs368861241
hgdp	rs368861241
ensembl	rs368861241
geneview	rs368861241
scholar	rs368861241
google	rs368861241
pharmgkb	rs368861241
gwascentral	rs368861241
openSNP	rs368861241
23andMe	rs368861241
SNPshot	rs368861241
SNPdbe	rs368861241
MSV3d	rs368861241
GWAS Ctlg	rs368861241

Max Magnitude

0

ClinVar
Risk	rs368861241(A;A)
Alt	rs368861241(A;A)
Reference	Rs368861241(G;G)
Significance	Other
Disease	Primary familial hypertrophic cardiomyopathy not specified not provided Hypertrophic cardiomyopathy
Variation	info
Gene	TNNI3
CLNDBN	Primary familial hypertrophic cardiomyopathy not specified not provided Hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000019.9:g.55665463G>A
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000148896.2, RCV000154211.1, RCV000159228.4, RCV000475238.1,