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: rs2014486
rs2014486 		1.000 0.040 11 1237573 intron variant A/G snv 0.52
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2075859
rs2075859 		11 1229258 missense variant C/G;T snv 0.39
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2672812
rs2672812 		11 1228142 intron variant G/A snv 0.51
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2735727
rs2735727 		11 1236229 intron variant G/A;C snv
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2735733
rs2735733 		1.000 0.040 11 1240410 intron variant C/T snv 0.49 0.43
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2857476
rs2857476 		1.000 0.040 11 1259904 intron variant T/C snv 0.54
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs4963059
rs4963059 		11 1251628 synonymous variant C/T snv 0.32 0.29
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs56293203
rs56293203 		1.000 0.040 11 1226857 missense variant G/A snv 9.2E-03 8.5E-03
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs868903
rs868903 		0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2014486
rs2014486 		1.000 0.040 11 1237573 intron variant A/G snv 0.52
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic 		Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2249073
rs2249073 		1.000 0.040 11 1252603 intron variant T/C snv 0.52
CUI: C0011334
Disease: Dental caries
Dental caries 		Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2735733
rs2735733 		1.000 0.040 11 1240410 intron variant C/T snv 0.49 0.43
CUI: C0011334
Disease: Dental caries
Dental caries 		Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2857476
rs2857476 		1.000 0.040 11 1259904 intron variant T/C snv 0.54
CUI: C0011334
Disease: Dental caries
Dental caries 		Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs868903
rs868903 		0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs868903
rs868903 		0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis 		Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs868903
rs868903 		0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010