rs727503697

Orientation

minus

Stabilized

minus

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

Make rs727503697(C;T)

Make rs727503697(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

178779055

Gene	LOC101927055, TTN

is a	snp
is	mentioned by
dbSNP	rs727503697
dbSNP (classic)	rs727503697
ClinGen	rs727503697
ebi	rs727503697
HLI	rs727503697
Exac	rs727503697
Gnomad	rs727503697
Varsome	rs727503697
LitVar	rs727503697
Map	rs727503697
PheGenI	rs727503697
Biobank	rs727503697
1000 genomes	rs727503697
hgdp	rs727503697
ensembl	rs727503697
geneview	rs727503697
scholar	rs727503697
google	rs727503697
pharmgkb	rs727503697
gwascentral	rs727503697
openSNP	rs727503697
23andMe	rs727503697
SNPshot	rs727503697
SNPdbe	rs727503697
MSV3d	rs727503697
GWAS Ctlg	rs727503697

Max Magnitude

0

ClinVar
Risk	rs727503697(T;T)
Alt	rs727503697(T;T)
Reference	Rs727503697(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN LOC101927055
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179643782G>A
CLNSRC
CLNACC	RCV000152508.1,