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rs1057520025

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520025(C;C)
Make rs1057520025(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28034144
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057520025
dbSNP (old)rs1057520025
ClinGenrs1057520025
ebirs1057520025
HLIrs1057520025
Exacrs1057520025
Gnomadrs1057520025
Varsomers1057520025
Maprs1057520025
PheGenIrs1057520025
Biobankrs1057520025
1000 genomesrs1057520025
hgdprs1057520025
ensemblrs1057520025
gopubmedrs1057520025
geneviewrs1057520025
scholarrs1057520025
googlers1057520025
pharmgkbrs1057520025
gwascentralrs1057520025
openSNPrs1057520025
23andMers1057520025
23andMe allrs1057520025
SNPshotrs1057520025
SNPdbers1057520025
MSV3drs1057520025
GWAS Ctlgrs1057520025
Max Magnitude0
ClinVar
Risk rs1057520025(C;C)
Alt rs1057520025(C;C)
Reference Rs1057520025(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28608281A>G
CLNSRC
CLNACC RCV000435462.1,