rs779874042
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs779874042(C;T) |
Make rs779874042(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178563493 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs779874042 |
dbSNP (classic) | rs779874042 |
ClinGen | rs779874042 |
ebi | rs779874042 |
HLI | rs779874042 |
Exac | rs779874042 |
Gnomad | rs779874042 |
Varsome | rs779874042 |
LitVar | rs779874042 |
Map | rs779874042 |
PheGenI | rs779874042 |
Biobank | rs779874042 |
1000 genomes | rs779874042 |
hgdp | rs779874042 |
ensembl | rs779874042 |
geneview | rs779874042 |
scholar | rs779874042 |
rs779874042 | |
pharmgkb | rs779874042 |
gwascentral | rs779874042 |
openSNP | rs779874042 |
23andMe | rs779874042 |
SNPshot | rs779874042 |
SNPdbe | rs779874042 |
MSV3d | rs779874042 |
GWAS Ctlg | rs779874042 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs779874042(A;A) rs779874042(T;T) |
Alt | rs779874042(A;A) rs779874042(T;T) |
Reference | Rs779874042(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.179428220C>A |
CLNSRC | |
CLNACC | RCV000184272.2, |