rs587782987
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587782987(C;T) |
Make rs587782987(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178611274 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs587782987 |
dbSNP (classic) | rs587782987 |
ClinGen | rs587782987 |
ebi | rs587782987 |
HLI | rs587782987 |
Exac | rs587782987 |
Gnomad | rs587782987 |
Varsome | rs587782987 |
LitVar | rs587782987 |
Map | rs587782987 |
PheGenI | rs587782987 |
Biobank | rs587782987 |
1000 genomes | rs587782987 |
hgdp | rs587782987 |
ensembl | rs587782987 |
geneview | rs587782987 |
scholar | rs587782987 |
rs587782987 | |
pharmgkb | rs587782987 |
gwascentral | rs587782987 |
openSNP | rs587782987 |
23andMe | rs587782987 |
SNPshot | rs587782987 |
SNPdbe | rs587782987 |
MSV3d | rs587782987 |
GWAS Ctlg | rs587782987 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782987(T;T) |
Alt | rs587782987(T;T) |
Reference | Rs587782987(C;C) |
Significance | Probable-Pathogenic |
Disease | Primary dilated cardiomyopathy not specified |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | Primary dilated cardiomyopathy not specified |
Reversed | 1 |
HGVS | NC_000002.11:g.179476001G>A |
CLNSRC | |
CLNACC | RCV000143972.2, RCV000225702.2, |