FLT3, fms related receptor tyrosine kinase 3, 2322

N. diseases: 270; N. variants: 54
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1933437
rs1933437 		13 28050157 missense variant G/A snv 0.60 0.53
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2018 2018
dbSNP: rs189992044
rs189992044 		13 28075859 intron variant C/A snv 3.8E-03
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs189992044
rs189992044 		13 28075859 intron variant C/A snv 3.8E-03
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs1933437
rs1933437 		13 28050157 missense variant G/A snv 0.60 0.53
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2504236
rs2504236 		13 28039161 intron variant C/T snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs34061361
rs34061361 		13 28044450 intron variant AAA/-;A;AA;AAAA delins
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs34061361
rs34061361 		13 28044450 intron variant AAA/-;A;AA;AAAA delins
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs34061361
rs34061361 		13 28044450 intron variant AAA/-;A;AA;AAAA delins
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs34061361
rs34061361 		13 28044450 intron variant AAA/-;A;AA;AAAA delins
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs34061361
rs34061361 		13 28044450 intron variant AAA/-;A;AA;AAAA delins
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs61946325
rs61946325 		13 28023050 intron variant C/T snv 0.16
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs61946325
rs61946325 		13 28023050 intron variant C/T snv 0.16
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs7318817
rs7318817 		13 28043571 intron variant C/T snv 0.61
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs772468040
rs772468040 		13 28057413 missense variant C/G;T snv 1.2E-05; 4.0E-06
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs772468040
rs772468040 		13 28057413 missense variant C/G;T snv 1.2E-05; 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs9507983
rs9507983 		13 28045899 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs9513008
rs9513008 		13 28053535 intron variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs9513018
rs9513018 		13 28066426 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9551434
rs9551434 		13 28067434 intron variant A/G snv 0.18
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2018 2018
dbSNP: rs9551434
rs9551434 		13 28067434 intron variant A/G snv 0.18
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs9554228
rs9554228 		13 28063701 intron variant A/G snv 0.60
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs9554228
rs9554228 		13 28063701 intron variant A/G snv 0.60
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs121913488
rs121913488 		0.807 0.120 13 28018505 missense variant C/A;G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.740 1.000 22 2001 2019
dbSNP: rs121913488
rs121913488 		0.807 0.120 13 28018505 missense variant C/A;G;T snv
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		Hemic and Lymphatic Diseases 0.010 1.000 1 2004 2004
dbSNP: rs121913488
rs121913488 		0.807 0.120 13 28018505 missense variant C/A;G;T snv
CUI: C3896960
Disease: Childhood Pre-B Acute Lymphoblastic Leukemia
Childhood Pre-B Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015