C1QTNF6, C1q and TNF related 6, 114904

N. diseases: 4; N. variants: 3
Source: GWASDB ×
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: rs229541
rs229541 		0.807 0.200 22 37195278 intron variant G/A snv 0.49
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.810 1.000 2 2008 2015
dbSNP: rs229527
rs229527 		0.925 0.160 22 37185445 missense variant C/A;G snv 0.43
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.810 1.000 1 2013 2017
dbSNP: rs229527
rs229527 		0.925 0.160 22 37185445 missense variant C/A;G snv 0.43
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.800 1.000 3 2010 2016
dbSNP: rs229526
rs229526 		1.000 0.120 22 37185382 missense variant G/C;T snv 0.19; 4.0E-06
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs229541
rs229541 		0.807 0.200 22 37195278 intron variant G/A snv 0.49
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011