rs397517497

Orientation

minus

Stabilized

minus

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

Make rs397517497(A;A)

Make rs397517497(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

178790707

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs397517497
dbSNP (classic)	rs397517497
ClinGen	rs397517497
ebi	rs397517497
HLI	rs397517497
Exac	rs397517497
Gnomad	rs397517497
Varsome	rs397517497
LitVar	rs397517497
Map	rs397517497
PheGenI	rs397517497
Biobank	rs397517497
1000 genomes	rs397517497
hgdp	rs397517497
ensembl	rs397517497
geneview	rs397517497
scholar	rs397517497
google	rs397517497
pharmgkb	rs397517497
gwascentral	rs397517497
openSNP	rs397517497
23andMe	rs397517497
SNPshot	rs397517497
SNPdbe	rs397517497
MSV3d	rs397517497
GWAS Ctlg	rs397517497

Max Magnitude

0

ClinVar
Risk	rs397517497(A;A)
Alt	rs397517497(A;A)
Reference	Rs397517497(G;G)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy not provided
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy not provided
Reversed	1
HGVS	NC_000002.11:g.179655434C>T
CLNSRC	ClinVar
CLNACC	RCV000039959.2, RCV000184208.1,