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: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2015 2015
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0024299
Disease: Lymphoma
Lymphoma 		0.010 1.000 1 2008 2008
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2015 2015
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C4721414
Disease: Mantle cell lymphoma
Mantle cell lymphoma 		0.010 1.000 1 2010 2010