rs727504782
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs727504782(-;-) |
Make rs727504782(-;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178562725 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs727504782 |
dbSNP (classic) | rs727504782 |
ClinGen | rs727504782 |
ebi | rs727504782 |
HLI | rs727504782 |
Exac | rs727504782 |
Gnomad | rs727504782 |
Varsome | rs727504782 |
LitVar | rs727504782 |
Map | rs727504782 |
PheGenI | rs727504782 |
Biobank | rs727504782 |
1000 genomes | rs727504782 |
hgdp | rs727504782 |
ensembl | rs727504782 |
geneview | rs727504782 |
scholar | rs727504782 |
rs727504782 | |
pharmgkb | rs727504782 |
gwascentral | rs727504782 |
openSNP | rs727504782 |
23andMe | rs727504782 |
SNPshot | rs727504782 |
SNPdbe | rs727504782 |
MSV3d | rs727504782 |
GWAS Ctlg | rs727504782 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727504782(-;-) |
Alt | rs727504782(-;-) |
Reference | Rs727504782(G;G) |
Significance | Probable-Pathogenic |
Disease | Primary dilated cardiomyopathy |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | Primary dilated cardiomyopathy |
Reversed | 1 |
HGVS | NC_000002.11:g.179427452delC |
CLNSRC | |
CLNACC | RCV000156100.1, |