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rs121913487

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913487(A;A)
Make rs121913487(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28018503
GeneFLT3
is asnp
is mentioned by
dbSNPrs121913487
dbSNP (old)rs121913487
ClinGenrs121913487
ebirs121913487
HLIrs121913487
Exacrs121913487
Gnomadrs121913487
Varsomers121913487
Maprs121913487
PheGenIrs121913487
Biobankrs121913487
1000 genomesrs121913487
hgdprs121913487
ensemblrs121913487
gopubmedrs121913487
geneviewrs121913487
scholarrs121913487
googlers121913487
pharmgkbrs121913487
gwascentralrs121913487
openSNPrs121913487
23andMers121913487
23andMe allrs121913487
SNPshotrs121913487
SNPdbers121913487
MSV3drs121913487
GWAS Ctlgrs121913487
Max Magnitude0
ClinVar
Risk rs121913487(A;A) rs121913487(G;G)
Alt rs121913487(A;A) rs121913487(G;G)
Reference Rs121913487(T;T)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592640A>C; NC_000013.10:g.28592640A>T
CLNSRC
CLNACC RCV000444148.1, RCV000424615.1,