IFI16, interferon gamma inducible protein 16, 3428

N. diseases: 79; N. variants: 14
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: rs4657616
rs4657616 		1 159001296 intron variant A/G snv 0.31
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.800 1.000 3 2011 2019
dbSNP: rs1772408
rs1772408 		1 159035859 intron variant A/G;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.800 1.000 1 2011 2011
dbSNP: rs1772408
rs1772408 		1 159035859 intron variant A/G;T snv
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		Immune System Diseases 0.800 1.000 1 2011 2011
dbSNP: rs1057024
rs1057024 		1 159020457 synonymous variant A/G snv 0.22 0.32
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs1101993
rs1101993 		1 159027105 intron variant G/A snv 0.65
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs2570916
rs2570916 		1 159042856 intron variant C/G;T snv 0.62
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs4657616
rs4657616 		1 159001296 intron variant A/G snv 0.31
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2013 2013
dbSNP: rs72709516
rs72709516 		1 159035061 intron variant C/T snv 3.2E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs856049
rs856049 		1 159020622 intron variant A/G snv 0.63
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs856054
rs856054 		1 159031731 intron variant C/T snv 0.61
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs856064
rs856064 		1 159013495 intron variant T/C snv 0.63
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs861318
rs861318 		1 159032432 intron variant A/G snv 0.70
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs1057028
rs1057028 		1.000 0.040 1 159032599 missense variant T/A snv 0.78 0.70
CUI: C4025886
Disease: Severe periodontitis
Severe periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1101998
rs1101998 		1.000 0.040 1 159029494 intron variant C/T snv 0.65
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2020 2020
dbSNP: rs1633256
rs1633256 		1.000 0.040 1 159032767 intron variant A/G snv 0.70
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2020 2020
dbSNP: rs6940
rs6940 		1.000 0.200 1 159054878 missense variant A/T snv 0.15 0.17
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2015 2015