Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs772061268
rs772061268
FLT3
1.000 0.040 13 28018487 missense variant T/G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2006 2006
dbSNP: rs991132188
rs991132188
FLT3
1.000 0.040 13 28018492 missense variant T/C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2005 2005
dbSNP: rs121909646
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.700 0
dbSNP: rs121913488
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.700 0
dbSNP: rs398122514
rs398122514
FLT3
1.000 0.040 13 28018487 inframe insertion -/TCCGGA delins 4.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 0
dbSNP: rs587776834
rs587776834
FLT3
1.000 0.120 13 28034140 inframe deletion TCA/- delins
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.700 0