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: rs1920116
rs1920116
0.882 0.040 3 169862183 intron variant G/A snv 0.25
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.820 1.000 2 2014 2015
dbSNP: rs1920116
rs1920116
0.882 0.040 3 169862183 intron variant G/A snv 0.25
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
Neoplasms; Nervous System Diseases 0.800 1.000 1 2014 2014
dbSNP: rs11709840
rs11709840
1.000 0.160 3 169852453 intron variant A/C snv 0.28
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11919269
rs11919269
1.000 0.160 3 169856677 intron variant T/G snv 0.35 0.28
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13074500
rs13074500
1.000 0.160 3 169847783 intron variant T/C snv 0.24
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs16854453
rs16854453
1.000 0.160 3 169841446 intron variant G/A snv 0.25
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1920116
rs1920116
0.882 0.040 3 169862183 intron variant G/A snv 0.25
CUI: C4722099
Disease: High grade glioma
High grade glioma
Neoplasms 0.020 1.000 2 2014 2015
dbSNP: rs1920116
rs1920116
0.882 0.040 3 169862183 intron variant G/A snv 0.25
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma
Neoplasms 0.020 1.000 2 2014 2015
dbSNP: rs16847897
rs16847897
0.851 0.320 3 169850328 intron variant G/A;C snv
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs16847897
rs16847897
0.851 0.320 3 169850328 intron variant G/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs16847897
rs16847897
0.851 0.320 3 169850328 intron variant G/A;C snv
CUI: C0004277
Disease: Tooth Attrition
Tooth Attrition
Stomatognathic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs16847897
rs16847897
0.851 0.320 3 169850328 intron variant G/A;C snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1920116
rs1920116
0.882 0.040 3 169862183 intron variant G/A snv 0.25
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2015 2015