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rs121909646

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909646(A;T)
Make rs121909646(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position28018504
GeneFLT3
is asnp
is mentioned by
dbSNPrs121909646
ebirs121909646
HLIrs121909646
Exacrs121909646
Varsomers121909646
Maprs121909646
PheGenIrs121909646
hapmaprs121909646
1000 genomesrs121909646
hgdprs121909646
ensemblrs121909646
gopubmedrs121909646
geneviewrs121909646
scholarrs121909646
googlers121909646
pharmgkbrs121909646
gwascentralrs121909646
openSNPrs121909646
23andMers121909646
23andMe allrs121909646
SNP Nexus

SNPshotrs121909646
SNPdbers121909646
MSV3drs121909646
GWAS Ctlgrs121909646
Max Magnitude0
OMIM136351
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909646(T;T)
Alt rs121909646(T;T)
Reference rs121909646(A;A)
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.28592641T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017660.5, RCV000017661.5,