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: rs13259407
rs13259407
1.000 0.040 8 18565413 intron variant C/T snv 0.47
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs150639459
rs150639459
1.000 0.040 8 18947176 intron variant C/A;T snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs2638663
rs2638663
8 18816221 intron variant T/C;G snv 0.53
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2013 2013
dbSNP: rs76185967
rs76185967
8 18774816 non coding transcript exon variant C/T snv 1.6E-02
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2019 2019
dbSNP: rs76185967
rs76185967
8 18774816 non coding transcript exon variant C/T snv 1.6E-02
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2019 2019
dbSNP: rs876983
rs876983
1.000 0.040 8 18550348 intron variant T/C snv 0.40
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs969599
rs969599
0.851 0.080 8 18567221 intron variant G/A;T snv
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs969599
rs969599
0.851 0.080 8 18567221 intron variant G/A;T snv
Amyotrophic Lateral Sclerosis, Sporadic
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs969599
rs969599
0.851 0.080 8 18567221 intron variant G/A;T snv
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs969599
rs969599
0.851 0.080 8 18567221 intron variant G/A;T snv
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
0.700 1.000 1 2016 2016
dbSNP: rs12156368
rs12156368
0.925 0.120 8 18885203 intron variant C/T snv 0.36
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12156368
rs12156368
0.925 0.120 8 18885203 intron variant C/T snv 0.36
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs13254772
rs13254772
1.000 0.080 8 18718646 intron variant T/A;C snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4921966
rs4921966
1.000 0.080 8 18840908 intron variant G/T snv 0.35
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6983992
rs6983992
0.925 0.120 8 18871125 intron variant T/C snv 0.20
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6983992
rs6983992
0.925 0.120 8 18871125 intron variant T/C snv 0.20
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7009615
rs7009615
1.000 0.080 8 18715325 intron variant T/C snv 0.21
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7843239
rs7843239
0.925 0.120 8 18884539 intron variant G/A snv 0.17
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7843239
rs7843239
0.925 0.120 8 18884539 intron variant G/A snv 0.17
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017