rs869025556

Orientation

minus

Stabilized

minus

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

Make rs869025556(-;A)

Make rs869025556(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178740362

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs869025556
dbSNP (classic)	rs869025556
ClinGen	rs869025556
ebi	rs869025556
HLI	rs869025556
Exac	rs869025556
Gnomad	rs869025556
Varsome	rs869025556
LitVar	rs869025556
Map	rs869025556
PheGenI	rs869025556
Biobank	rs869025556
1000 genomes	rs869025556
hgdp	rs869025556
ensembl	rs869025556
geneview	rs869025556
scholar	rs869025556
google	rs869025556
pharmgkb	rs869025556
gwascentral	rs869025556
openSNP	rs869025556
23andMe	rs869025556
SNPshot	rs869025556
SNPdbe	rs869025556
MSV3d	rs869025556
GWAS Ctlg	rs869025556

Max Magnitude

0

ClinVar
Risk	rs869025556(A;A)
Alt	rs869025556(A;A)
Reference	Rs869025556(-;-)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy Cardiovascular phenotype not specified
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy Cardiovascular phenotype not specified
Reversed	1
HGVS	NC_000002.11:g.179605090dupT
CLNSRC
CLNACC	RCV000207997.1, RCV000243632.1, RCV000480182.1,