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rs1057520022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520022(C;C)
Make rs1057520022(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28034183
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057520022
dbSNP (old)rs1057520022
ClinGenrs1057520022
ebirs1057520022
HLIrs1057520022
Exacrs1057520022
Gnomadrs1057520022
Varsomers1057520022
Maprs1057520022
PheGenIrs1057520022
Biobankrs1057520022
1000 genomesrs1057520022
hgdprs1057520022
ensemblrs1057520022
gopubmedrs1057520022
geneviewrs1057520022
scholarrs1057520022
googlers1057520022
pharmgkbrs1057520022
gwascentralrs1057520022
openSNPrs1057520022
23andMers1057520022
23andMe allrs1057520022
SNPshotrs1057520022
SNPdbers1057520022
MSV3drs1057520022
GWAS Ctlgrs1057520022
Max Magnitude0
ClinVar
Risk rs1057520022(C;C)
Alt rs1057520022(C;C)
Reference Rs1057520022(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28608320A>G
CLNSRC
CLNACC RCV000445102.1,