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rs1057519767

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519767(A;G)
Make rs1057519767(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28028205
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057519767
dbSNP (old)rs1057519767
ClinGenrs1057519767
ebirs1057519767
HLIrs1057519767
Exacrs1057519767
Gnomadrs1057519767
Varsomers1057519767
Maprs1057519767
PheGenIrs1057519767
Biobankrs1057519767
1000 genomesrs1057519767
hgdprs1057519767
ensemblrs1057519767
gopubmedrs1057519767
geneviewrs1057519767
scholarrs1057519767
googlers1057519767
pharmgkbrs1057519767
gwascentralrs1057519767
openSNPrs1057519767
23andMers1057519767
23andMe allrs1057519767
SNPshotrs1057519767
SNPdbers1057519767
MSV3drs1057519767
GWAS Ctlgrs1057519767
Max Magnitude0
ClinVar
Risk rs1057519767(G;G)
Alt rs1057519767(G;G)
Reference Rs1057519767(A;A)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28602342T>C
CLNSRC
CLNACC RCV000443164.1,