rs876657663

Orientation

minus

Stabilized

minus

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

Make rs876657663(-;-)

Make rs876657663(-;ACACGTT)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178759040

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs876657663
dbSNP (classic)	rs876657663
ClinGen	rs876657663
ebi	rs876657663
HLI	rs876657663
Exac	rs876657663
Gnomad	rs876657663
Varsome	rs876657663
LitVar	rs876657663
Map	rs876657663
PheGenI	rs876657663
Biobank	rs876657663
1000 genomes	rs876657663
hgdp	rs876657663
ensembl	rs876657663
geneview	rs876657663
scholar	rs876657663
google	rs876657663
pharmgkb	rs876657663
gwascentral	rs876657663
openSNP	rs876657663
23andMe	rs876657663
SNPshot	rs876657663
SNPdbe	rs876657663
MSV3d	rs876657663
GWAS Ctlg	rs876657663

Max Magnitude

0

ClinVar
Risk	rs876657663(-;-)
Alt	rs876657663(-;-)
Reference	Rs876657663(ACACGTT;ACACGTT)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179623767_179623773delAACGTGT
CLNSRC
CLNACC	RCV000214597.1,