rs869312105

Orientation

minus

Stabilized

minus

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

Make rs869312105(G;G)

Make rs869312105(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178635489

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs869312105
dbSNP (classic)	rs869312105
ClinGen	rs869312105
ebi	rs869312105
HLI	rs869312105
Exac	rs869312105
Gnomad	rs869312105
Varsome	rs869312105
LitVar	rs869312105
Map	rs869312105
PheGenI	rs869312105
Biobank	rs869312105
1000 genomes	rs869312105
hgdp	rs869312105
ensembl	rs869312105
geneview	rs869312105
scholar	rs869312105
google	rs869312105
pharmgkb	rs869312105
gwascentral	rs869312105
openSNP	rs869312105
23andMe	rs869312105
SNPshot	rs869312105
SNPdbe	rs869312105
MSV3d	rs869312105
GWAS Ctlg	rs869312105

Max Magnitude

0

ClinVar
Risk	rs869312105(G;G)
Alt	rs869312105(G;G)
Reference	Rs869312105(T;T)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179500216A>C
CLNSRC
CLNACC	RCV000208928.1,