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rs121913486

From SNPedia

Orientationminus
Geno Mag Summary
(GAT;GAT) 0 common in clinvar
Make rs121913486(-;-)
Make rs121913486(-;GAT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position28018503
GeneFLT3
is asnp
is mentioned by
dbSNPrs121913486
ebirs121913486
HLIrs121913486
Exacrs121913486
Varsomers121913486
Maprs121913486
PheGenIrs121913486
hapmaprs121913486
1000 genomesrs121913486
hgdprs121913486
ensemblrs121913486
gopubmedrs121913486
geneviewrs121913486
scholarrs121913486
googlers121913486
pharmgkbrs121913486
gwascentralrs121913486
openSNPrs121913486
23andMers121913486
23andMe allrs121913486
SNP Nexus

SNPshotrs121913486
SNPdbers121913486
MSV3drs121913486
GWAS Ctlgrs121913486
Max Magnitude0
ClinVar
Risk rs121913486(;)
Alt rs121913486(;)
Reference rs121913486(GAT;GAT)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592640_28592642delATC
CLNSRC OMIM Allelic Variant
CLNACC RCV000017667.6,