rs111692981

Orientation

plus

Stabilized

plus

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

Make rs111692981(A;A)

Make rs111692981(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

201359257

Gene

TNNT2

is a	snp
is	mentioned by
dbSNP	rs111692981
dbSNP (classic)	rs111692981
ClinGen	rs111692981
ebi	rs111692981
HLI	rs111692981
Exac	rs111692981
Gnomad	rs111692981
Varsome	rs111692981
LitVar	rs111692981
Map	rs111692981
PheGenI	rs111692981
Biobank	rs111692981
1000 genomes	rs111692981
hgdp	rs111692981
ensembl	rs111692981
geneview	rs111692981
scholar	rs111692981
google	rs111692981
pharmgkb	rs111692981
gwascentral	rs111692981
openSNP	rs111692981
23andMe	rs111692981
SNPshot	rs111692981
SNPdbe	rs111692981
MSV3d	rs111692981
GWAS Ctlg	rs111692981

Max Magnitude

0

ClinVar
Risk	rs111692981(A;A) rs111692981(C;C) rs111692981(G;G)
Alt	rs111692981(A;A) rs111692981(C;C) rs111692981(G;G)
Reference	Rs111692981(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TNNT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.201328385T>G
CLNSRC
CLNACC	RCV000484808.1,