rs769392594
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs769392594(G;G) |
Make rs769392594(G;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178608256 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs769392594 |
dbSNP (classic) | rs769392594 |
ClinGen | rs769392594 |
ebi | rs769392594 |
HLI | rs769392594 |
Exac | rs769392594 |
Gnomad | rs769392594 |
Varsome | rs769392594 |
LitVar | rs769392594 |
Map | rs769392594 |
PheGenI | rs769392594 |
Biobank | rs769392594 |
1000 genomes | rs769392594 |
hgdp | rs769392594 |
ensembl | rs769392594 |
geneview | rs769392594 |
scholar | rs769392594 |
rs769392594 | |
pharmgkb | rs769392594 |
gwascentral | rs769392594 |
openSNP | rs769392594 |
23andMe | rs769392594 |
SNPshot | rs769392594 |
SNPdbe | rs769392594 |
MSV3d | rs769392594 |
GWAS Ctlg | rs769392594 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769392594(A;A) rs769392594(G;G) |
Alt | rs769392594(A;A) rs769392594(G;G) |
Reference | Rs769392594(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.179472983T>A |
CLNSRC | |
CLNACC | RCV000184234.1, |