rs141805127

Orientation

plus

Stabilized

plus

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

Make rs141805127(C;T)

Make rs141805127(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

201361314

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs141805127
dbSNP (classic)	rs141805127
ClinGen	rs141805127
ebi	rs141805127
HLI	rs141805127
Exac	rs141805127
Gnomad	rs141805127
Varsome	rs141805127
LitVar	rs141805127
Map	rs141805127
PheGenI	rs141805127
Biobank	rs141805127
1000 genomes	rs141805127
hgdp	rs141805127
ensembl	rs141805127
geneview	rs141805127
scholar	rs141805127
google	rs141805127
pharmgkb	rs141805127
gwascentral	rs141805127
openSNP	rs141805127
23andMe	rs141805127
SNPshot	rs141805127
SNPdbe	rs141805127
MSV3d	rs141805127
GWAS Ctlg	rs141805127

Max Magnitude

0

ClinVar
Risk	rs141805127(T;T)
Alt	rs141805127(T;T)
Reference	Rs141805127(C;C)
Significance	Other
Disease	not provided Familial hypertrophic cardiomyopathy 2 Familial restrictive cardiomyopathy 3 Left ventricular noncompaction 6
Variation	info
Gene	TNNT2
CLNDBN	not provided Familial hypertrophic cardiomyopathy 2 Familial restrictive cardiomyopathy 3 Left ventricular noncompaction 6
Reversed	0
HGVS	NC_000001.10:g.201330442C>T
CLNSRC
CLNACC	RCV000172136.2, RCV000466482.1,