rs727503636

Orientation

minus

Stabilized

minus

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

Make rs727503636(A;A)

Make rs727503636(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

178689052

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs727503636
dbSNP (classic)	rs727503636
ClinGen	rs727503636
ebi	rs727503636
HLI	rs727503636
Exac	rs727503636
Gnomad	rs727503636
Varsome	rs727503636
LitVar	rs727503636
Map	rs727503636
PheGenI	rs727503636
Biobank	rs727503636
1000 genomes	rs727503636
hgdp	rs727503636
ensembl	rs727503636
geneview	rs727503636
scholar	rs727503636
google	rs727503636
pharmgkb	rs727503636
gwascentral	rs727503636
openSNP	rs727503636
23andMe	rs727503636
SNPshot	rs727503636
SNPdbe	rs727503636
MSV3d	rs727503636
GWAS Ctlg	rs727503636

Max Magnitude

0

ClinVar
Risk	rs727503636(A;A)
Alt	rs727503636(A;A)
Reference	Rs727503636(G;G)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy not specified
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy not specified
Reversed	1
HGVS	NC_000002.11:g.179553779C>T
CLNSRC
CLNACC	RCV000152375.1, RCV000184202.2,