rs869312041

Orientation

minus

Stabilized

minus

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

Make rs869312041(-;-)

Make rs869312041(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178682904

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs869312041
dbSNP (classic)	rs869312041
ClinGen	rs869312041
ebi	rs869312041
HLI	rs869312041
Exac	rs869312041
Gnomad	rs869312041
Varsome	rs869312041
LitVar	rs869312041
Map	rs869312041
PheGenI	rs869312041
Biobank	rs869312041
1000 genomes	rs869312041
hgdp	rs869312041
ensembl	rs869312041
geneview	rs869312041
scholar	rs869312041
google	rs869312041
pharmgkb	rs869312041
gwascentral	rs869312041
openSNP	rs869312041
23andMe	rs869312041
SNPshot	rs869312041
SNPdbe	rs869312041
MSV3d	rs869312041
GWAS Ctlg	rs869312041

Max Magnitude

0

ClinVar
Risk	rs869312041(-;-)
Alt	rs869312041(-;-)
Reference	Rs869312041(G;G)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179547631delC
CLNSRC
CLNACC	RCV000209671.1,