rs267607158

Orientation

minus

Stabilized

minus

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

Make rs267607158(C;T)

Make rs267607158(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

178740125

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs267607158
ClinGen	rs267607158
ebi	rs267607158
HLI	rs267607158
Exac	rs267607158
Varsome	rs267607158
Map	rs267607158
PheGenI	rs267607158
hapmap	rs267607158
1000 genomes	rs267607158
hgdp	rs267607158
ensembl	rs267607158
gopubmed	rs267607158
geneview	rs267607158
scholar	rs267607158
google	rs267607158
pharmgkb	rs267607158
gwascentral	rs267607158
openSNP	rs267607158
23andMe	rs267607158
23andMe all	rs267607158
SNP Nexus
SNPshot	rs267607158
SNPdbe	rs267607158
MSV3d	rs267607158
GWAS Ctlg	rs267607158

Max Magnitude

0

ClinVar
Risk	rs267607158(T;T)
Alt	rs267607158(T;T)
Reference	Rs267607158(C;C)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 1G
Variation	info
Gene	TTN
CLNDBN	Dilated cardiomyopathy 1G
Reversed	1
HGVS	NC_000002.11:g.179604852G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013493.18,