rs876657668
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs876657668(C;C) |
Make rs876657668(C;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 178585348 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs876657668 |
dbSNP (classic) | rs876657668 |
ClinGen | rs876657668 |
ebi | rs876657668 |
HLI | rs876657668 |
Exac | rs876657668 |
Gnomad | rs876657668 |
Varsome | rs876657668 |
LitVar | rs876657668 |
Map | rs876657668 |
PheGenI | rs876657668 |
Biobank | rs876657668 |
1000 genomes | rs876657668 |
hgdp | rs876657668 |
ensembl | rs876657668 |
geneview | rs876657668 |
scholar | rs876657668 |
rs876657668 | |
pharmgkb | rs876657668 |
gwascentral | rs876657668 |
openSNP | rs876657668 |
23andMe | rs876657668 |
SNPshot | rs876657668 |
SNPdbe | rs876657668 |
MSV3d | rs876657668 |
GWAS Ctlg | rs876657668 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657668(C;C) |
Alt | rs876657668(C;C) |
Reference | Rs876657668(G;G) |
Significance | Probable-Pathogenic |
Disease | Primary dilated cardiomyopathy |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | Primary dilated cardiomyopathy |
Reversed | 1 |
HGVS | NC_000002.11:g.179450075C>G |
CLNSRC | |
CLNACC | RCV000222488.1, |