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rs1057519766

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519766(C;G)
Make rs1057519766(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28028203
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519766
dbSNP (old)rs1057519766
ClinGenrs1057519766
ebirs1057519766
HLIrs1057519766
Exacrs1057519766
Gnomadrs1057519766
Varsomers1057519766
Maprs1057519766
PheGenIrs1057519766
Biobankrs1057519766
1000 genomesrs1057519766
hgdprs1057519766
ensemblrs1057519766
gopubmedrs1057519766
geneviewrs1057519766
scholarrs1057519766
googlers1057519766
pharmgkbrs1057519766
gwascentralrs1057519766
openSNPrs1057519766
23andMers1057519766
23andMe allrs1057519766
SNP Nexus

SNPshotrs1057519766
SNPdbers1057519766
MSV3drs1057519766
GWAS Ctlgrs1057519766
Max Magnitude0
ClinVar
Risk rs1057519766(A;A) rs1057519766(G;G)
Alt rs1057519766(A;A) rs1057519766(G;G)
Reference Rs1057519766(C;C)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28602340G>C; NC_000013.10:g.28602340G>T
CLNSRC
CLNACC RCV000427705.1, RCV000434039.1,