rs1057519160

Orientation

minus

Stabilized

minus

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

Make rs1057519160(A;A)

Make rs1057519160(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

178711235

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs1057519160
dbSNP (classic)	rs1057519160
ClinGen	rs1057519160
ebi	rs1057519160
HLI	rs1057519160
Exac	rs1057519160
Gnomad	rs1057519160
Varsome	rs1057519160
LitVar	rs1057519160
Map	rs1057519160
PheGenI	rs1057519160
Biobank	rs1057519160
1000 genomes	rs1057519160
hgdp	rs1057519160
ensembl	rs1057519160
geneview	rs1057519160
scholar	rs1057519160
google	rs1057519160
pharmgkb	rs1057519160
gwascentral	rs1057519160
openSNP	rs1057519160
23andMe	rs1057519160
SNPshot	rs1057519160
SNPdbe	rs1057519160
MSV3d	rs1057519160
GWAS Ctlg	rs1057519160

Max Magnitude

0

ClinVar
Risk	rs1057519160(A;A)
Alt	rs1057519160(A;A)
Reference	Rs1057519160(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TTN
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.179575962C>T
CLNSRC
CLNACC	RCV000416209.2,