rs121964860

Orientation

minus

Stabilized

minus

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

Make rs121964860(G;T)

Make rs121964860(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201361988

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs121964860
dbSNP (classic)	rs121964860
ClinGen	rs121964860
ebi	rs121964860
HLI	rs121964860
Exac	rs121964860
Gnomad	rs121964860
Varsome	rs121964860
LitVar	rs121964860
Map	rs121964860
PheGenI	rs121964860
Biobank	rs121964860
1000 genomes	rs121964860
hgdp	rs121964860
ensembl	rs121964860
geneview	rs121964860
scholar	rs121964860
google	rs121964860
pharmgkb	rs121964860
gwascentral	rs121964860
openSNP	rs121964860
23andMe	rs121964860
SNPshot	rs121964860
SNPdbe	rs121964860
MSV3d	rs121964860
GWAS Ctlg	rs121964860

Max Magnitude

0

OMIM	191045
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121964860(A;A) rs121964860(C;C) rs121964860(T;T)
Alt	rs121964860(A;A) rs121964860(C;C) rs121964860(T;T)
Reference	Rs121964860(G;G)
Significance	Pathogenic
Disease	Left ventricular noncompaction 6 not specified
Variation	info
Gene	TNNT2
CLNDBN	Left ventricular noncompaction 6 not specified
Reversed	1
HGVS	NC_000001.10:g.201331116C>A; NC_000001.10:g.201331116C>G; NC_000001.10:g.201331116C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013228.24, RCV000220074.1, RCV000152098.1, RCV000464711.1,