rs1057518065

Orientation

minus

Stabilized

minus

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

Make rs1057518065(-;-)

Make rs1057518065(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

178624617

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs1057518065
dbSNP (classic)	rs1057518065
ClinGen	rs1057518065
ebi	rs1057518065
HLI	rs1057518065
Exac	rs1057518065
Gnomad	rs1057518065
Varsome	rs1057518065
LitVar	rs1057518065
Map	rs1057518065
PheGenI	rs1057518065
Biobank	rs1057518065
1000 genomes	rs1057518065
hgdp	rs1057518065
ensembl	rs1057518065
geneview	rs1057518065
scholar	rs1057518065
google	rs1057518065
pharmgkb	rs1057518065
gwascentral	rs1057518065
openSNP	rs1057518065
23andMe	rs1057518065
SNPshot	rs1057518065
SNPdbe	rs1057518065
MSV3d	rs1057518065
GWAS Ctlg	rs1057518065

Max Magnitude

0

ClinVar
Risk	rs1057518065(-;-)
Alt	rs1057518065(-;-)
Reference	Rs1057518065(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TTN
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.179489344delT
CLNSRC
CLNACC	RCV000414635.1,