rs121964859

Merged into

rs45578238

Orientation

minus

Stabilized

minus

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

Make rs121964859(-;-)

Make rs121964859(-;AAG)

Make rs121964859(AAG;AAG)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201361972

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs121964859
dbSNP (classic)	rs121964859
ClinGen	rs121964859
ebi	rs121964859
HLI	rs121964859
Exac	rs121964859
Gnomad	rs121964859
Varsome	rs121964859
LitVar	rs121964859
Map	rs121964859
PheGenI	rs121964859
Biobank	rs121964859
1000 genomes	rs121964859
hgdp	rs121964859
ensembl	rs121964859
geneview	rs121964859
scholar	rs121964859
google	rs121964859
pharmgkb	rs121964859
gwascentral	rs121964859
openSNP	rs121964859
23andMe	rs121964859
SNPshot	rs121964859
SNPdbe	rs121964859
MSV3d	rs121964859
GWAS Ctlg	rs121964859

Status

Merged into rs45578238

Max Magnitude

0

OMIM	191045
Desc
Variant	0006
Related	also

ClinVar
Risk
Alt
Reference	Rs121964859(AGA;AGA)
Significance	Pathogenic
Disease	Left ventricular noncompaction 6 Cardiomyopathy Familial hypertrophic cardiomyopathy 2 Primary dilated cardiomyopathy not provided
Variation	info
Gene	TNNT2
CLNDBN	Left ventricular noncompaction 6 Cardiomyopathy Familial hypertrophic cardiomyopathy 2 Primary dilated cardiomyopathy not provided
Reversed	1
HGVS	NC_000001.10:g.201331099_201331101delTCT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000036607.4, RCV000159333.1, RCV000168972.1, RCV000211868.1, RCV000223828.1,