MX1, MX dynamin like GTPase 1, 4599

N. diseases: 71; N. variants: 7
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: rs17000900
rs17000900 		0.925 0.120 21 41426103 5 prime UTR variant C/A snv 0.14
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.020 1.000 2 2007 2017
dbSNP: rs17000900
rs17000900 		0.925 0.120 21 41426103 5 prime UTR variant C/A snv 0.14
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs2071430
rs2071430 		0.807 0.320 21 41426138 5 prime UTR variant G/T snv 0.15
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs2071430
rs2071430 		0.807 0.320 21 41426138 5 prime UTR variant G/T snv 0.15
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs2071430
rs2071430 		0.807 0.320 21 41426138 5 prime UTR variant G/T snv 0.15
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2071430
rs2071430 		0.807 0.320 21 41426138 5 prime UTR variant G/T snv 0.15
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2071430
rs2071430 		0.807 0.320 21 41426138 5 prime UTR variant G/T snv 0.15
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2071430
rs2071430 		0.807 0.320 21 41426138 5 prime UTR variant G/T snv 0.15
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2071430
rs2071430 		0.807 0.320 21 41426138 5 prime UTR variant G/T snv 0.15
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs457274
rs457274 		1.000 0.040 21 41420558 5 prime UTR variant C/G snv 0.35
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs457274
rs457274 		1.000 0.040 21 41420558 5 prime UTR variant C/G snv 0.35
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs461093
rs461093 		1.000 0.080 21 41428263 non coding transcript exon variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs464138
rs464138 		1.000 0.080 21 41426246 5 prime UTR variant A/C snv 0.36
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs469083
rs469083 		1.000 0.040 21 41436789 intron variant C/T snv 0.61
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs469083
rs469083 		1.000 0.040 21 41436789 intron variant C/T snv 0.61
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs763554423
rs763554423 		1.000 0.080 21 41441838 missense variant G/A snv 4.0E-06
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2009 2009