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rs1057519762

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519762(C;C)
Make rs1057519762(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28018484
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519762
dbSNP (old)rs1057519762
ClinGenrs1057519762
ebirs1057519762
HLIrs1057519762
Exacrs1057519762
Gnomadrs1057519762
Varsomers1057519762
Maprs1057519762
PheGenIrs1057519762
Biobankrs1057519762
1000 genomesrs1057519762
hgdprs1057519762
ensemblrs1057519762
gopubmedrs1057519762
geneviewrs1057519762
scholarrs1057519762
googlers1057519762
pharmgkbrs1057519762
gwascentralrs1057519762
openSNPrs1057519762
23andMers1057519762
23andMe allrs1057519762
SNPshotrs1057519762
SNPdbers1057519762
MSV3drs1057519762
GWAS Ctlgrs1057519762
Max Magnitude0
ClinVar
Risk rs1057519762(C;C)
Alt rs1057519762(C;C)
Reference Rs1057519762(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592621A>G
CLNSRC
CLNACC RCV000431811.1,