Source: GWASCAT

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: rs11931598
rs11931598
TADA2B ; LOC100129931
4 7045375 intron variant C/T snv 0.55
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs11931598
rs11931598
TADA2B ; LOC100129931
4 7045375 intron variant C/T snv 0.55
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs11931598
rs11931598
TADA2B ; LOC100129931
4 7045375 intron variant C/T snv 0.55
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11931598
rs11931598
TADA2B ; LOC100129931
4 7045375 intron variant C/T snv 0.55
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs568868093
rs568868093
TADA2B ; CCDC96 ; LOC100129931
4 7043344 intron variant CGG/-;CGGCGG;CGGCGGCGG;CGGCGGCGGCGG;CGGCGGCGGCGGCGG delins
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs568868093
rs568868093
TADA2B ; CCDC96 ; LOC100129931
4 7043344 intron variant CGG/-;CGGCGG;CGGCGGCGG;CGGCGGCGGCGG;CGGCGGCGGCGGCGG delins
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016