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rs1057520043

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520043(G;G)
Make rs1057520043(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28034148
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057520043
dbSNP (old)rs1057520043
ClinGenrs1057520043
ebirs1057520043
HLIrs1057520043
Exacrs1057520043
Gnomadrs1057520043
Varsomers1057520043
Maprs1057520043
PheGenIrs1057520043
Biobankrs1057520043
1000 genomesrs1057520043
hgdprs1057520043
ensemblrs1057520043
gopubmedrs1057520043
geneviewrs1057520043
scholarrs1057520043
googlers1057520043
pharmgkbrs1057520043
gwascentralrs1057520043
openSNPrs1057520043
23andMers1057520043
23andMe allrs1057520043
SNPshotrs1057520043
SNPdbers1057520043
MSV3drs1057520043
GWAS Ctlgrs1057520043
Max Magnitude0
ClinVar
Risk rs1057520043(G;G)
Alt rs1057520043(G;G)
Reference Rs1057520043(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28608285A>C
CLNSRC
CLNACC RCV000441431.1,