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: rs117739035
rs117739035 		1.000 0.040 11 408174 missense variant G/T snv 2.9E-02 2.5E-02
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
Necrotizing enterocolitis in fetus OR newborn 		Digestive System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3210908
rs3210908 		1.000 0.080 11 406483 missense variant T/A;C snv 0.84
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs7396562
rs7396562 		1.000 0.080 11 408352 intron variant C/A snv 0.21
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs766709278
rs766709278 		1.000 0.040 11 407546 stop gained G/C snv 8.4E-06 2.1E-05
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
Necrotizing enterocolitis in fetus OR newborn 		Digestive System Diseases 0.010 1.000 1 2015 2015