rs869312044

Orientation

minus

Stabilized

minus

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

Make rs869312044(-;-)

Make rs869312044(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178631256

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs869312044
dbSNP (classic)	rs869312044
ClinGen	rs869312044
ebi	rs869312044
HLI	rs869312044
Exac	rs869312044
Gnomad	rs869312044
Varsome	rs869312044
LitVar	rs869312044
Map	rs869312044
PheGenI	rs869312044
Biobank	rs869312044
1000 genomes	rs869312044
hgdp	rs869312044
ensembl	rs869312044
geneview	rs869312044
scholar	rs869312044
google	rs869312044
pharmgkb	rs869312044
gwascentral	rs869312044
openSNP	rs869312044
23andMe	rs869312044
SNPshot	rs869312044
SNPdbe	rs869312044
MSV3d	rs869312044
GWAS Ctlg	rs869312044

Max Magnitude

0

ClinVar
Risk	rs869312044(-;-)
Alt	rs869312044(-;-)
Reference	Rs869312044(G;G)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179495983delC
CLNSRC
CLNACC	RCV000209396.1,