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rs1057519726

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519726(A;C)
Make rs1057519726(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28018502
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519726
dbSNP (old)rs1057519726
ClinGenrs1057519726
ebirs1057519726
HLIrs1057519726
Exacrs1057519726
Gnomadrs1057519726
Varsomers1057519726
Maprs1057519726
PheGenIrs1057519726
Biobankrs1057519726
1000 genomesrs1057519726
hgdprs1057519726
ensemblrs1057519726
gopubmedrs1057519726
geneviewrs1057519726
scholarrs1057519726
googlers1057519726
pharmgkbrs1057519726
gwascentralrs1057519726
openSNPrs1057519726
23andMers1057519726
23andMe allrs1057519726
SNPshotrs1057519726
SNPdbers1057519726
MSV3drs1057519726
GWAS Ctlgrs1057519726
Max Magnitude0
ClinVar
Risk rs1057519726(C;C) rs1057519726(G;G) rs1057519726(T;T)
Alt rs1057519726(C;C) rs1057519726(G;G) rs1057519726(T;T)
Reference Rs1057519726(A;A)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592639T>A; NC_000013.10:g.28592639T>C; NC_000013.10:g.28592639T>G
CLNSRC
CLNACC RCV000417837.1, RCV000428691.1, RCV000432941.1,