rs771562210

Orientation

plus

Stabilized

plus

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

Make rs771562210(C;T)

Make rs771562210(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

178630240

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs771562210
dbSNP (classic)	rs771562210
ClinGen	rs771562210
ebi	rs771562210
HLI	rs771562210
Exac	rs771562210
Gnomad	rs771562210
Varsome	rs771562210
LitVar	rs771562210
Map	rs771562210
PheGenI	rs771562210
Biobank	rs771562210
1000 genomes	rs771562210
hgdp	rs771562210
ensembl	rs771562210
geneview	rs771562210
scholar	rs771562210
google	rs771562210
pharmgkb	rs771562210
gwascentral	rs771562210
openSNP	rs771562210
23andMe	rs771562210
SNPshot	rs771562210
SNPdbe	rs771562210
MSV3d	rs771562210
GWAS Ctlg	rs771562210

Max Magnitude

0

ClinVar
Risk	rs771562210(T;T)
Alt	rs771562210(T;T)
Reference	Rs771562210(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy Dilated cardiomyopathy 1G Limb-girdle muscular dystrophy
Variation	info
Gene	TTN
CLNDBN	Primary dilated cardiomyopathy Dilated cardiomyopathy 1G Limb-girdle muscular dystrophy, type 2J
Reversed	0
HGVS	NC_000002.11:g.179494967C>T
CLNSRC
CLNACC	RCV000209118.1, RCV000459817.1,