rs794729358
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs794729358(-;-) |
Make rs794729358(-;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 178557442 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs794729358 |
dbSNP (classic) | rs794729358 |
ClinGen | rs794729358 |
ebi | rs794729358 |
HLI | rs794729358 |
Exac | rs794729358 |
Gnomad | rs794729358 |
Varsome | rs794729358 |
LitVar | rs794729358 |
Map | rs794729358 |
PheGenI | rs794729358 |
Biobank | rs794729358 |
1000 genomes | rs794729358 |
hgdp | rs794729358 |
ensembl | rs794729358 |
geneview | rs794729358 |
scholar | rs794729358 |
rs794729358 | |
pharmgkb | rs794729358 |
gwascentral | rs794729358 |
openSNP | rs794729358 |
23andMe | rs794729358 |
SNPshot | rs794729358 |
SNPdbe | rs794729358 |
MSV3d | rs794729358 |
GWAS Ctlg | rs794729358 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794729358(-;-) |
Alt | rs794729358(-;-) |
Reference | Rs794729358(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.179422169delG |
CLNSRC | |
CLNACC | RCV000184351.2, |