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rs1057519763

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1057519763(GA;TT)
Make rs1057519763(TT;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28018504
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519763
dbSNP (old)rs1057519763
ClinGenrs1057519763
ebirs1057519763
HLIrs1057519763
Exacrs1057519763
Gnomadrs1057519763
Varsomers1057519763
Maprs1057519763
PheGenIrs1057519763
Biobankrs1057519763
1000 genomesrs1057519763
hgdprs1057519763
ensemblrs1057519763
gopubmedrs1057519763
geneviewrs1057519763
scholarrs1057519763
googlers1057519763
pharmgkbrs1057519763
gwascentralrs1057519763
openSNPrs1057519763
23andMers1057519763
23andMe allrs1057519763
SNPshotrs1057519763
SNPdbers1057519763
MSV3drs1057519763
GWAS Ctlgrs1057519763
Max Magnitude0
ClinVar
Risk rs1057519763(TT;TT)
Alt rs1057519763(TT;TT)
Reference Rs1057519763(GA;GA)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592641_28592642delTCinsAA
CLNSRC
CLNACC RCV000439080.1,