rs397517698

Orientation

minus

Stabilized

minus

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

Make rs397517698(-;-)

Make rs397517698(-;AAAG)

Reference

GRCh38 38.1/141

Chromosome

2

Position

178775030

Gene	LOC101927055, TTN

is a	snp
is	mentioned by
dbSNP	rs397517698
dbSNP (classic)	rs397517698
ClinGen	rs397517698
ebi	rs397517698
HLI	rs397517698
Exac	rs397517698
Gnomad	rs397517698
Varsome	rs397517698
LitVar	rs397517698
Map	rs397517698
PheGenI	rs397517698
Biobank	rs397517698
1000 genomes	rs397517698
hgdp	rs397517698
ensembl	rs397517698
geneview	rs397517698
scholar	rs397517698
google	rs397517698
pharmgkb	rs397517698
gwascentral	rs397517698
openSNP	rs397517698
23andMe	rs397517698
SNPshot	rs397517698
SNPdbe	rs397517698
MSV3d	rs397517698
GWAS Ctlg	rs397517698

Max Magnitude

0

ClinVar
Risk	rs397517698(-;-)
Alt	rs397517698(-;-)
Reference	Rs397517698(AAAG;AAAG)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	TTN LOC101927055
CLNDBN	Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000002.11:g.179639757_179639760delCTTT
CLNSRC	ClinVar
CLNACC	RCV000040597.2,