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rs1057519768

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519768(A;G)
Make rs1057519768(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28028279
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519768
dbSNP (classic)rs1057519768
ClinGenrs1057519768
ebirs1057519768
HLIrs1057519768
Exacrs1057519768
Gnomadrs1057519768
Varsomers1057519768
LitVarrs1057519768
Maprs1057519768
PheGenIrs1057519768
Biobankrs1057519768
1000 genomesrs1057519768
hgdprs1057519768
ensemblrs1057519768
geneviewrs1057519768
scholarrs1057519768
googlers1057519768
pharmgkbrs1057519768
gwascentralrs1057519768
openSNPrs1057519768
23andMers1057519768
23andMe allrs1057519768
SNPshotrs1057519768
SNPdbers1057519768
MSV3drs1057519768
GWAS Ctlgrs1057519768
Max Magnitude0
ClinVar
Risk rs1057519768(G;G)
Alt rs1057519768(G;G)
Reference Rs1057519768(A;A)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28602416T>C
CLNSRC
CLNACC RCV000426662.1,