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: rs2270450
rs2270450 		0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs2270450
rs2270450 		0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs2270450
rs2270450 		0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs10807344
rs10807344 		0.925 0.120 6 46657898 intron variant C/T snv 0.17
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10807344
rs10807344 		0.925 0.120 6 46657898 intron variant C/T snv 0.17
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs2270450
rs2270450 		0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2270450
rs2270450 		0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs9472817
rs9472817 		0.882 0.080 6 46673255 intron variant C/G;T snv
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs9472817
rs9472817 		0.882 0.080 6 46673255 intron variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs9472817
rs9472817 		0.882 0.080 6 46673255 intron variant C/G;T snv
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2016 2016