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rs1057519769

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519769(G;T)
Make rs1057519769(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28033974
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519769
dbSNP (old)rs1057519769
ClinGenrs1057519769
ebirs1057519769
HLIrs1057519769
Exacrs1057519769
Gnomadrs1057519769
Varsomers1057519769
Maprs1057519769
PheGenIrs1057519769
Biobankrs1057519769
1000 genomesrs1057519769
hgdprs1057519769
ensemblrs1057519769
gopubmedrs1057519769
geneviewrs1057519769
scholarrs1057519769
googlers1057519769
pharmgkbrs1057519769
gwascentralrs1057519769
openSNPrs1057519769
23andMers1057519769
23andMe allrs1057519769
SNPshotrs1057519769
SNPdbers1057519769
MSV3drs1057519769
GWAS Ctlgrs1057519769
Max Magnitude0
ClinVar
Risk rs1057519769(T;T)
Alt rs1057519769(T;T)
Reference Rs1057519769(G;G)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28608111C>A
CLNSRC
CLNACC RCV000437384.1,