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rs1057519765

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519765(A;T)
Make rs1057519765(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28027236
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519765
dbSNP (old)rs1057519765
ClinGenrs1057519765
ebirs1057519765
HLIrs1057519765
Exacrs1057519765
Gnomadrs1057519765
Varsomers1057519765
Maprs1057519765
PheGenIrs1057519765
Biobankrs1057519765
1000 genomesrs1057519765
hgdprs1057519765
ensemblrs1057519765
gopubmedrs1057519765
geneviewrs1057519765
scholarrs1057519765
googlers1057519765
pharmgkbrs1057519765
gwascentralrs1057519765
openSNPrs1057519765
23andMers1057519765
23andMe allrs1057519765
SNPshotrs1057519765
SNPdbers1057519765
MSV3drs1057519765
GWAS Ctlgrs1057519765
Max Magnitude0
ClinVar
Risk rs1057519765(T;T)
Alt rs1057519765(T;T)
Reference Rs1057519765(A;A)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28601373T>A
CLNSRC
CLNACC RCV000443196.1,