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rs1057520023

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520023(G;G)
Make rs1057520023(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28018501
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057520023
dbSNP (old)rs1057520023
ClinGenrs1057520023
ebirs1057520023
HLIrs1057520023
Exacrs1057520023
Gnomadrs1057520023
Varsomers1057520023
LitVarrs1057520023
Maprs1057520023
PheGenIrs1057520023
Biobankrs1057520023
1000 genomesrs1057520023
hgdprs1057520023
ensemblrs1057520023
gopubmedrs1057520023
geneviewrs1057520023
scholarrs1057520023
googlers1057520023
pharmgkbrs1057520023
gwascentralrs1057520023
openSNPrs1057520023
23andMers1057520023
23andMe allrs1057520023
SNPshotrs1057520023
SNPdbers1057520023
MSV3drs1057520023
GWAS Ctlgrs1057520023
Max Magnitude0
ClinVar
Risk rs1057520023(G;G)
Alt rs1057520023(G;G)
Reference Rs1057520023(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592638A>C
CLNSRC
CLNACC RCV000444162.1,