rs756715989
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs756715989(C;T) |
Make rs756715989(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178580230 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs756715989 |
dbSNP (classic) | rs756715989 |
ClinGen | rs756715989 |
ebi | rs756715989 |
HLI | rs756715989 |
Exac | rs756715989 |
Gnomad | rs756715989 |
Varsome | rs756715989 |
LitVar | rs756715989 |
Map | rs756715989 |
PheGenI | rs756715989 |
Biobank | rs756715989 |
1000 genomes | rs756715989 |
hgdp | rs756715989 |
ensembl | rs756715989 |
geneview | rs756715989 |
scholar | rs756715989 |
rs756715989 | |
pharmgkb | rs756715989 |
gwascentral | rs756715989 |
openSNP | rs756715989 |
23andMe | rs756715989 |
SNPshot | rs756715989 |
SNPdbe | rs756715989 |
MSV3d | rs756715989 |
GWAS Ctlg | rs756715989 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756715989(G;G) rs756715989(T;T) |
Alt | rs756715989(G;G) rs756715989(T;T) |
Reference | Rs756715989(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.179444957C>G |
CLNSRC | |
CLNACC | RCV000184388.1, |