rs769488730
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TTTAA;TTTAA) | 0 | common in clinvar |
Make rs769488730(-;-) |
Make rs769488730(-;TTTAA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178547519 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs769488730 |
dbSNP (classic) | rs769488730 |
ClinGen | rs769488730 |
ebi | rs769488730 |
HLI | rs769488730 |
Exac | rs769488730 |
Gnomad | rs769488730 |
Varsome | rs769488730 |
LitVar | rs769488730 |
Map | rs769488730 |
PheGenI | rs769488730 |
Biobank | rs769488730 |
1000 genomes | rs769488730 |
hgdp | rs769488730 |
ensembl | rs769488730 |
geneview | rs769488730 |
scholar | rs769488730 |
rs769488730 | |
pharmgkb | rs769488730 |
gwascentral | rs769488730 |
openSNP | rs769488730 |
23andMe | rs769488730 |
SNPshot | rs769488730 |
SNPdbe | rs769488730 |
MSV3d | rs769488730 |
GWAS Ctlg | rs769488730 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769488730(-;-) |
Alt | rs769488730(-;-) |
Reference | Rs769488730(TTTAA;TTTAA) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.179412246_179412250delTTTAA |
CLNSRC | |
CLNACC | RCV000184360.2, |