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: rs374234147
rs374234147
FLT3
1.000 0.040 13 28057443 missense variant T/C snv 4.0E-06 7.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.010 1.000 1 2013 2013
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: rs3829382
rs3829382
FLT3
0.925 0.040 13 28003551 3 prime UTR variant G/T snv 0.46
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.010 1.000 1 2013 2013
dbSNP: rs3829382
rs3829382
FLT3
0.925 0.040 13 28003551 3 prime UTR variant G/T snv 0.46
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		0.010 1.000 1 2013 2013
dbSNP: rs759272576
rs759272576
FLT3
1.000 0.040 13 28027224 missense variant A/G snv 4.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.010 1.000 1 2019 2019
dbSNP: rs762392769
rs762392769
FLT3
1.000 0.040 13 28018553 missense variant C/T snv 8.0E-06
CUI: C0023530
Disease: Leukopenia
Leukopenia 		0.010 1.000 1 2009 2009
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