rs121913488
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121913488(C;C) |
Make rs121913488(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 28018505 |
Gene | FLT3 |
is a | snp |
is | mentioned by |
dbSNP | rs121913488 |
dbSNP (classic) | rs121913488 |
ClinGen | rs121913488 |
ebi | rs121913488 |
HLI | rs121913488 |
Exac | rs121913488 |
Gnomad | rs121913488 |
Varsome | rs121913488 |
LitVar | rs121913488 |
Map | rs121913488 |
PheGenI | rs121913488 |
Biobank | rs121913488 |
1000 genomes | rs121913488 |
hgdp | rs121913488 |
ensembl | rs121913488 |
geneview | rs121913488 |
scholar | rs121913488 |
rs121913488 | |
pharmgkb | rs121913488 |
gwascentral | rs121913488 |
openSNP | rs121913488 |
23andMe | rs121913488 |
SNPshot | rs121913488 |
SNPdbe | rs121913488 |
MSV3d | rs121913488 |
GWAS Ctlg | rs121913488 |
Merged from | Rs121909647, Rs121909648, Rs121909649 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913488(A;A) rs121913488(C;C) rs121913488(T;T) |
Alt | rs121913488(A;A) rs121913488(C;C) rs121913488(T;T) |
Reference | Rs121913488(G;G) |
Significance | Pathogenic |
Disease | Acute myeloid leukemia Acute lymphoid leukemia |
Variation | info |
Gene | FLT3 |
CLNDBN | Acute myeloid leukemia Acute lymphoid leukemia |
Reversed | 1 |
HGVS | NC_000013.10:g.28592642C>A; NC_000013.10:g.28592642C>G; NC_000013.10:g.28592642C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017665.5, RCV000017666.4, RCV000017662.6, RCV000017663.6, |