rs750955319
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs750955319(A;A) |
Make rs750955319(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 20 |
Position | 32428404 |
Gene | ASXL1 |
is a | snp |
is | mentioned by |
dbSNP | rs750955319 |
dbSNP (classic) | rs750955319 |
ClinGen | rs750955319 |
ebi | rs750955319 |
HLI | rs750955319 |
Exac | rs750955319 |
Gnomad | rs750955319 |
Varsome | rs750955319 |
LitVar | rs750955319 |
Map | rs750955319 |
PheGenI | rs750955319 |
Biobank | rs750955319 |
1000 genomes | rs750955319 |
hgdp | rs750955319 |
ensembl | rs750955319 |
geneview | rs750955319 |
scholar | rs750955319 |
rs750955319 | |
pharmgkb | rs750955319 |
gwascentral | rs750955319 |
openSNP | rs750955319 |
23andMe | rs750955319 |
SNPshot | rs750955319 |
SNPdbe | rs750955319 |
MSV3d | rs750955319 |
GWAS Ctlg | rs750955319 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs750955319(A;A) |
Alt | rs750955319(A;A) |
Reference | Rs750955319(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | ASXL1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000020.10:g.31016207C>A |
CLNSRC | |
CLNACC | RCV000171344.2, |