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: rs121913490
rs121913490
FLT3
1.000 0.040 13 28018498 inframe deletion GAT/- delins
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2014 2014
dbSNP: rs121913491
rs121913491
FLT3
1.000 0.040 13 28034204 missense variant T/C snv 2.0E-05 7.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2014 2014
dbSNP: rs749281035
rs749281035
FLT3
1.000 0.040 13 28018485 missense variant G/A;T snv 4.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2005 2005
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: 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