rs869312102

Orientation

minus

Stabilized

minus

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

Make rs869312102(A;A)

Make rs869312102(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178741321

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs869312102
dbSNP (classic)	rs869312102
ClinGen	rs869312102
ebi	rs869312102
HLI	rs869312102
Exac	rs869312102
Gnomad	rs869312102
Varsome	rs869312102
LitVar	rs869312102
Map	rs869312102
PheGenI	rs869312102
Biobank	rs869312102
1000 genomes	rs869312102
hgdp	rs869312102
ensembl	rs869312102
geneview	rs869312102
scholar	rs869312102
google	rs869312102
pharmgkb	rs869312102
gwascentral	rs869312102
openSNP	rs869312102
23andMe	rs869312102
SNPshot	rs869312102
SNPdbe	rs869312102
MSV3d	rs869312102
GWAS Ctlg	rs869312102

Max Magnitude

0

ClinVar
Risk	rs869312102(A;A)
Alt	rs869312102(A;A)
Reference	Rs869312102(G;G)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179606048C>T
CLNSRC
CLNACC	RCV000209746.1,