rs542568224
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs542568224(C;T) |
Make rs542568224(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 20 |
Position | 32436347 |
Gene | ASXL1 |
is a | snp |
is | mentioned by |
dbSNP | rs542568224 |
dbSNP (classic) | rs542568224 |
ClinGen | rs542568224 |
ebi | rs542568224 |
HLI | rs542568224 |
Exac | rs542568224 |
Gnomad | rs542568224 |
Varsome | rs542568224 |
LitVar | rs542568224 |
Map | rs542568224 |
PheGenI | rs542568224 |
Biobank | rs542568224 |
1000 genomes | rs542568224 |
hgdp | rs542568224 |
ensembl | rs542568224 |
geneview | rs542568224 |
scholar | rs542568224 |
rs542568224 | |
pharmgkb | rs542568224 |
gwascentral | rs542568224 |
openSNP | rs542568224 |
23andMe | rs542568224 |
SNPshot | rs542568224 |
SNPdbe | rs542568224 |
MSV3d | rs542568224 |
GWAS Ctlg | rs542568224 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs542568224(T;T) |
Alt | rs542568224(T;T) |
Reference | Rs542568224(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ASXL1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.31024150C>T |
CLNSRC | |
CLNACC | RCV000171346.1, |