rs869312079
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs869312079(-;-) |
Make rs869312079(-;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 178564614 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs869312079 |
dbSNP (classic) | rs869312079 |
ClinGen | rs869312079 |
ebi | rs869312079 |
HLI | rs869312079 |
Exac | rs869312079 |
Gnomad | rs869312079 |
Varsome | rs869312079 |
LitVar | rs869312079 |
Map | rs869312079 |
PheGenI | rs869312079 |
Biobank | rs869312079 |
1000 genomes | rs869312079 |
hgdp | rs869312079 |
ensembl | rs869312079 |
geneview | rs869312079 |
scholar | rs869312079 |
rs869312079 | |
pharmgkb | rs869312079 |
gwascentral | rs869312079 |
openSNP | rs869312079 |
23andMe | rs869312079 |
SNPshot | rs869312079 |
SNPdbe | rs869312079 |
MSV3d | rs869312079 |
GWAS Ctlg | rs869312079 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869312079(-;-) |
Alt | rs869312079(-;-) |
Reference | Rs869312079(C;C) |
Significance | Probable-Pathogenic |
Disease | Primary dilated cardiomyopathy |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | Primary dilated cardiomyopathy |
Reversed | 1 |
HGVS | NC_000002.11:g.179429341delG |
CLNSRC | |
CLNACC | RCV000208927.1, |