rs869312106

Orientation

minus

Stabilized

minus

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

Make rs869312106(-;-)

Make rs869312106(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178633863

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs869312106
dbSNP (classic)	rs869312106
ClinGen	rs869312106
ebi	rs869312106
HLI	rs869312106
Exac	rs869312106
Gnomad	rs869312106
Varsome	rs869312106
LitVar	rs869312106
Map	rs869312106
PheGenI	rs869312106
Biobank	rs869312106
1000 genomes	rs869312106
hgdp	rs869312106
ensembl	rs869312106
geneview	rs869312106
scholar	rs869312106
google	rs869312106
pharmgkb	rs869312106
gwascentral	rs869312106
openSNP	rs869312106
23andMe	rs869312106
SNPshot	rs869312106
SNPdbe	rs869312106
MSV3d	rs869312106
GWAS Ctlg	rs869312106

Max Magnitude

0

ClinVar
Risk	rs869312106(-;-)
Alt	rs869312106(-;-)
Reference	Rs869312106(A;A)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179498590delT
CLNSRC
CLNACC	RCV000209251.1,