rs76428106, FLT3

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 2 2016 2017
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 2 2016 2017
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 2 2016 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 1 2019 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 1 2019 2019
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 1 2019 2019
RDW - Red blood cell distribution width result
988 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 1 2019 2019
Red cell distribution width determination
988 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 1 2019 2019