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rs121913490

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAT;CAT) 0 common in clinvar
Make rs121913490(-;-)
Make rs121913490(-;ATC)
Make rs121913490(ATC;ATC)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28018500
GeneFLT3
is asnp
is mentioned by
dbSNPrs121913490
dbSNP (old)rs121913490
ClinGenrs121913490
ebirs121913490
HLIrs121913490
Exacrs121913490
Gnomadrs121913490
Varsomers121913490
Maprs121913490
PheGenIrs121913490
Biobankrs121913490
1000 genomesrs121913490
hgdprs121913490
ensemblrs121913490
gopubmedrs121913490
geneviewrs121913490
scholarrs121913490
googlers121913490
pharmgkbrs121913490
gwascentralrs121913490
openSNPrs121913490
23andMers121913490
23andMe allrs121913490
SNPshotrs121913490
SNPdbers121913490
MSV3drs121913490
GWAS Ctlgrs121913490
Max Magnitude0
ClinVar
Risk rs121913490(-;-)
Alt rs121913490(-;-)
Reference Rs121913490(CAT;CAT)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592637_28592639delGAT
CLNSRC
CLNACC RCV000424567.1,