rs559590585
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs559590585(C;T) |
Make rs559590585(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178608330 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs559590585 |
dbSNP (classic) | rs559590585 |
ClinGen | rs559590585 |
ebi | rs559590585 |
HLI | rs559590585 |
Exac | rs559590585 |
Gnomad | rs559590585 |
Varsome | rs559590585 |
LitVar | rs559590585 |
Map | rs559590585 |
PheGenI | rs559590585 |
Biobank | rs559590585 |
1000 genomes | rs559590585 |
hgdp | rs559590585 |
ensembl | rs559590585 |
geneview | rs559590585 |
scholar | rs559590585 |
rs559590585 | |
pharmgkb | rs559590585 |
gwascentral | rs559590585 |
openSNP | rs559590585 |
23andMe | rs559590585 |
SNPshot | rs559590585 |
SNPdbe | rs559590585 |
MSV3d | rs559590585 |
GWAS Ctlg | rs559590585 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs559590585(G;G) rs559590585(T;T) |
Alt | rs559590585(G;G) rs559590585(T;T) |
Reference | Rs559590585(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.179473057C>T |
CLNSRC | |
CLNACC | RCV000171319.1, RCV000343935.1, |