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rs1057519764

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519764(G;G)
Make rs1057519764(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28027222
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519764
dbSNP (old)rs1057519764
ClinGenrs1057519764
ebirs1057519764
HLIrs1057519764
Exacrs1057519764
Gnomadrs1057519764
Varsomers1057519764
Maprs1057519764
PheGenIrs1057519764
Biobankrs1057519764
1000 genomesrs1057519764
hgdprs1057519764
ensemblrs1057519764
gopubmedrs1057519764
geneviewrs1057519764
scholarrs1057519764
googlers1057519764
pharmgkbrs1057519764
gwascentralrs1057519764
openSNPrs1057519764
23andMers1057519764
23andMe allrs1057519764
SNP Nexus

SNPshotrs1057519764
SNPdbers1057519764
MSV3drs1057519764
GWAS Ctlgrs1057519764
Max Magnitude0
ClinVar
Risk rs1057519764(A;A) rs1057519764(G;G)
Alt rs1057519764(A;A) rs1057519764(G;G)
Reference Rs1057519764(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28601359A>C; NC_000013.10:g.28601359A>T
CLNSRC
CLNACC RCV000420978.1, RCV000431699.1,