rs1057519237

Orientation

minus

Stabilized

minus

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

Make rs1057519237(C;T)

Make rs1057519237(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

178702634

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs1057519237
dbSNP (classic)	rs1057519237
ClinGen	rs1057519237
ebi	rs1057519237
HLI	rs1057519237
Exac	rs1057519237
Gnomad	rs1057519237
Varsome	rs1057519237
LitVar	rs1057519237
Map	rs1057519237
PheGenI	rs1057519237
Biobank	rs1057519237
1000 genomes	rs1057519237
hgdp	rs1057519237
ensembl	rs1057519237
geneview	rs1057519237
scholar	rs1057519237
google	rs1057519237
pharmgkb	rs1057519237
gwascentral	rs1057519237
openSNP	rs1057519237
23andMe	rs1057519237
SNPshot	rs1057519237
SNPdbe	rs1057519237
MSV3d	rs1057519237
GWAS Ctlg	rs1057519237

Max Magnitude

0

ClinVar
Risk	rs1057519237(T;T)
Alt	rs1057519237(T;T)
Reference	Rs1057519237(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TTN
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.179567361G>A
CLNSRC
CLNACC	RCV000415992.1,