rs121964861

Orientation

minus

Stabilized

minus

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

Make rs121964861(A;A)

Make rs121964861(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

201359636

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs121964861
dbSNP (classic)	rs121964861
ClinGen	rs121964861
ebi	rs121964861
HLI	rs121964861
Exac	rs121964861
Gnomad	rs121964861
Varsome	rs121964861
LitVar	rs121964861
Map	rs121964861
PheGenI	rs121964861
Biobank	rs121964861
1000 genomes	rs121964861
hgdp	rs121964861
ensembl	rs121964861
geneview	rs121964861
scholar	rs121964861
google	rs121964861
pharmgkb	rs121964861
gwascentral	rs121964861
openSNP	rs121964861
23andMe	rs121964861
SNPshot	rs121964861
SNPdbe	rs121964861
MSV3d	rs121964861
GWAS Ctlg	rs121964861

Max Magnitude

0

OMIM	191045
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121964861(A;A) rs121964861(T;T)
Alt	rs121964861(A;A) rs121964861(T;T)
Reference	Rs121964861(G;G)
Significance	Pathogenic
Disease	Left ventricular noncompaction 6
Variation	info
Gene	TNNT2
CLNDBN	Left ventricular noncompaction 6
Reversed	1
HGVS	NC_000001.10:g.201328764C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013229.22,