rs869312061
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs869312061(-;-) |
Make rs869312061(-;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 178559491 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs869312061 |
dbSNP (classic) | rs869312061 |
ClinGen | rs869312061 |
ebi | rs869312061 |
HLI | rs869312061 |
Exac | rs869312061 |
Gnomad | rs869312061 |
Varsome | rs869312061 |
LitVar | rs869312061 |
Map | rs869312061 |
PheGenI | rs869312061 |
Biobank | rs869312061 |
1000 genomes | rs869312061 |
hgdp | rs869312061 |
ensembl | rs869312061 |
geneview | rs869312061 |
scholar | rs869312061 |
rs869312061 | |
pharmgkb | rs869312061 |
gwascentral | rs869312061 |
openSNP | rs869312061 |
23andMe | rs869312061 |
SNPshot | rs869312061 |
SNPdbe | rs869312061 |
MSV3d | rs869312061 |
GWAS Ctlg | rs869312061 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869312061(-;-) |
Alt | rs869312061(-;-) |
Reference | Rs869312061(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.179424218delG |
CLNSRC | |
CLNACC | RCV000209817.1, |