Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520026

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520026(A;C)
Make rs1057520026(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28028244
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057520026
dbSNP (old)rs1057520026
ClinGenrs1057520026
ebirs1057520026
HLIrs1057520026
Exacrs1057520026
Gnomadrs1057520026
Varsomers1057520026
Maprs1057520026
PheGenIrs1057520026
Biobankrs1057520026
1000 genomesrs1057520026
hgdprs1057520026
ensemblrs1057520026
gopubmedrs1057520026
geneviewrs1057520026
scholarrs1057520026
googlers1057520026
pharmgkbrs1057520026
gwascentralrs1057520026
openSNPrs1057520026
23andMers1057520026
23andMe allrs1057520026
SNPshotrs1057520026
SNPdbers1057520026
MSV3drs1057520026
GWAS Ctlgrs1057520026
Max Magnitude0
ClinVar
Risk rs1057520026(C;C)
Alt rs1057520026(C;C)
Reference Rs1057520026(A;A)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28602381T>G
CLNSRC
CLNACC RCV000422333.1,