rs869312046

Orientation

minus

Stabilized

minus

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

Make rs869312046(G;G)

Make rs869312046(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178620798

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs869312046
dbSNP (classic)	rs869312046
ClinGen	rs869312046
ebi	rs869312046
HLI	rs869312046
Exac	rs869312046
Gnomad	rs869312046
Varsome	rs869312046
LitVar	rs869312046
Map	rs869312046
PheGenI	rs869312046
Biobank	rs869312046
1000 genomes	rs869312046
hgdp	rs869312046
ensembl	rs869312046
geneview	rs869312046
scholar	rs869312046
google	rs869312046
pharmgkb	rs869312046
gwascentral	rs869312046
openSNP	rs869312046
23andMe	rs869312046
SNPshot	rs869312046
SNPdbe	rs869312046
MSV3d	rs869312046
GWAS Ctlg	rs869312046

Max Magnitude

0

ClinVar
Risk	rs869312046(G;G)
Alt	rs869312046(G;G)
Reference	Rs869312046(T;T)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179485525A>C
CLNSRC
CLNACC	RCV000209593.1,