rs781171206
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs781171206(A;A) |
Make rs781171206(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178543276 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs781171206 |
dbSNP (classic) | rs781171206 |
ClinGen | rs781171206 |
ebi | rs781171206 |
HLI | rs781171206 |
Exac | rs781171206 |
Gnomad | rs781171206 |
Varsome | rs781171206 |
LitVar | rs781171206 |
Map | rs781171206 |
PheGenI | rs781171206 |
Biobank | rs781171206 |
1000 genomes | rs781171206 |
hgdp | rs781171206 |
ensembl | rs781171206 |
geneview | rs781171206 |
scholar | rs781171206 |
rs781171206 | |
pharmgkb | rs781171206 |
gwascentral | rs781171206 |
openSNP | rs781171206 |
23andMe | rs781171206 |
SNPshot | rs781171206 |
SNPdbe | rs781171206 |
MSV3d | rs781171206 |
GWAS Ctlg | rs781171206 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs781171206(A;A) |
Alt | rs781171206(A;A) |
Reference | Rs781171206(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.179408003G>A |
CLNSRC | |
CLNACC | RCV000184397.1, |