rs886041485
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Chromosome | 20 |
Position | 32433742 |
Gene | ASXL1 |
is a | snp |
is | mentioned by |
dbSNP | rs886041485 |
dbSNP (classic) | rs886041485 |
ClinGen | rs886041485 |
ebi | rs886041485 |
HLI | rs886041485 |
Exac | rs886041485 |
Gnomad | rs886041485 |
Varsome | rs886041485 |
LitVar | rs886041485 |
Map | rs886041485 |
PheGenI | rs886041485 |
Biobank | rs886041485 |
1000 genomes | rs886041485 |
hgdp | rs886041485 |
ensembl | rs886041485 |
geneview | rs886041485 |
scholar | rs886041485 |
rs886041485 | |
pharmgkb | rs886041485 |
gwascentral | rs886041485 |
openSNP | rs886041485 |
23andMe | rs886041485 |
SNPshot | rs886041485 |
SNPdbe | rs886041485 |
MSV3d | rs886041485 |
GWAS Ctlg | rs886041485 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041485(-;-) |
Alt | rs886041485(-;-) |
Reference | Rs886041485(TG;TG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ASXL1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.31021545_31021546delTG |
CLNSRC | |
CLNACC | RCV000366685.1, |