Source: BEFREE

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: rs772468040
rs772468040
FLT3
13 28057413 missense variant C/G;T snv 1.2E-05; 4.0E-06
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs772468040
rs772468040
FLT3
13 28057413 missense variant C/G;T snv 1.2E-05; 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs9513008
rs9513008
FLT3
13 28053535 intron variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs1057519764
rs1057519764
FLT3
1.000 0.040 13 28027222 missense variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.710 1.000 1 2012 2019
dbSNP: rs1057520026
rs1057520026
FLT3
0.925 0.040 13 28028244 missense variant T/G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.710 1.000 1 2006 2006
dbSNP: rs121913232
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.710 1.000 1 2003 2014
dbSNP: rs376588714
rs376588714
FLT3
1.000 0.040 13 28018483 missense variant T/C snv 2.4E-05 1.4E-05
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.710 1.000 1 2005 2014
dbSNP: rs1057519766
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.720 1.000 2 2013 2016
dbSNP: rs121913488
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.740 1.000 4 2001 2019