rs559063155
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs559063155(A;A) |
Make rs559063155(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 197402110 |
Gene | SF3B1 |
is a | snp |
is | mentioned by |
dbSNP | rs559063155 |
dbSNP (classic) | rs559063155 |
ClinGen | rs559063155 |
ebi | rs559063155 |
HLI | rs559063155 |
Exac | rs559063155 |
Gnomad | rs559063155 |
Varsome | rs559063155 |
LitVar | rs559063155 |
Map | rs559063155 |
PheGenI | rs559063155 |
Biobank | rs559063155 |
1000 genomes | rs559063155 |
hgdp | rs559063155 |
ensembl | rs559063155 |
geneview | rs559063155 |
scholar | rs559063155 |
rs559063155 | |
pharmgkb | rs559063155 |
gwascentral | rs559063155 |
openSNP | rs559063155 |
23andMe | rs559063155 |
SNPshot | rs559063155 |
SNPdbe | rs559063155 |
MSV3d | rs559063155 |
GWAS Ctlg | rs559063155 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs559063155(A;A) rs559063155(C;C) rs559063155(G;G) |
Alt | rs559063155(A;A) rs559063155(C;C) rs559063155(G;G) |
Reference | Rs559063155(T;T) |
Significance | Probable-Pathogenic |
Disease | Acute myeloid leukemia |
Variation | info |
Gene | SF3B1 |
CLNDBN | Acute myeloid leukemia |
Reversed | 0 |
HGVS | NC_000002.11:g.198266834T>A; NC_000002.11:g.198266834T>C; NC_000002.11:g.198266834T>G |
CLNSRC | |
CLNACC | RCV000424424.1, RCV000420863.1, RCV000435126.1, |