rs397517565

Orientation

minus

Stabilized

minus

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

Make rs397517565(-;-)

Make rs397517565(-;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

178635714

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs397517565
dbSNP (classic)	rs397517565
ClinGen	rs397517565
ebi	rs397517565
HLI	rs397517565
Exac	rs397517565
Gnomad	rs397517565
Varsome	rs397517565
LitVar	rs397517565
Map	rs397517565
PheGenI	rs397517565
Biobank	rs397517565
1000 genomes	rs397517565
hgdp	rs397517565
ensembl	rs397517565
geneview	rs397517565
scholar	rs397517565
google	rs397517565
pharmgkb	rs397517565
gwascentral	rs397517565
openSNP	rs397517565
23andMe	rs397517565
SNPshot	rs397517565
SNPdbe	rs397517565
MSV3d	rs397517565
GWAS Ctlg	rs397517565

Max Magnitude

0

ClinVar
Risk	rs397517565(-;-)
Alt	rs397517565(-;-)
Reference	Rs397517565(A;A)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy not provided
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy not provided
Reversed	1
HGVS	NC_000002.11:g.179500441delT
CLNSRC	ClinVar
CLNACC	RCV000040217.2, RCV000184297.1,