IL37, interleukin 37, 27178

N. diseases: 280; N. variants: 27
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: rs2708965
rs2708965 		2 112911501 upstream gene variant C/A snv 0.10
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723168
rs2723168 		2 112913313 intron variant G/A snv 9.8E-02
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723169
rs2723169 		2 112912904 upstream gene variant G/C snv 9.9E-02
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723175
rs2723175 		1.000 0.080 2 112910176 upstream gene variant G/A snv 0.11
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723177
rs2723177 		2 112914991 intron variant A/G snv 0.10
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723183
rs2723183 		1.000 0.040 2 112917144 missense variant A/G snv 6.8E-02 1.0E-01
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723187
rs2723187 		1.000 0.040 2 112917692 missense variant C/T snv 6.8E-02 1.0E-01
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723189
rs2723189 		2 112917851 intron variant G/A snv 1.0E-01
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2723192
rs2723192 		2 112918804 missense variant G/A;C;T snv 6.8E-02; 4.0E-06; 4.0E-06
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3811046
rs3811046 		0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3811046
rs3811046 		0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3811046
rs3811046 		0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71
CUI: C0080233
Disease: Tooth Loss
Tooth Loss 		Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3811046
rs3811046 		0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3811047
rs3811047 		0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3811047
rs3811047 		0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4458215
rs4458215 		2 112919378 downstream gene variant T/C snv 0.17
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1335908042
rs1335908042 		0.925 0.120 2 112918756 missense variant T/G snv 4.0E-06
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1335908042
rs1335908042 		0.925 0.120 2 112918756 missense variant T/G snv 4.0E-06
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2723175
rs2723175 		1.000 0.080 2 112910176 upstream gene variant G/A snv 0.11
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs2723176
rs2723176 		0.851 0.200 2 112914932 intron variant A/C;G snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs2723176
rs2723176 		0.851 0.200 2 112914932 intron variant A/C;G snv
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer 		Digestive System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs2723183
rs2723183 		1.000 0.040 2 112917144 missense variant A/G snv 6.8E-02 1.0E-01
CUI: C0031099
Disease: Periodontitis
Periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2020 2020
dbSNP: rs3811047
rs3811047 		0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer 		Digestive System Diseases 0.010 1.000 1 2020 2020