CD38, CD38 molecule, 952

N. diseases: 473; 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: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.030 1.000 3 2010 2012
dbSNP: rs1800561
rs1800561 		0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 0.500 2 2001 2015
dbSNP: rs1800561
rs1800561 		0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.020 1.000 2 2010 2012
dbSNP: rs1800561
rs1800561 		0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.020 0.500 2 2001 2015
dbSNP: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C0015458
Disease: Facial Hemiatrophy
Facial Hemiatrophy 		Nervous System Diseases; Stomatognathic Diseases 0.020 1.000 2 2010 2012
dbSNP: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C3840214
Disease: High-functioning autism
High-functioning autism 		Mental Disorders 0.020 1.000 2 2010 2012
dbSNP: rs6449182
rs6449182 		0.807 0.160 4 15778830 intron variant C/G snv 0.22
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2009 2012
dbSNP: rs13104011
rs13104011 		1.000 0.040 4 15805410 intron variant C/T snv 0.15
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		Behavior and Behavior Mechanisms 0.010 1.000 1 2014 2014
dbSNP: rs1800561
rs1800561 		0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1800561
rs1800561 		0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 1998 1998
dbSNP: rs1800561
rs1800561 		0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
B-CELL MALIGNANCY, LOW-GRADE 		0.010 1.000 1 2009 2009
dbSNP: rs1800561
rs1800561 		0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs368295543
rs368295543 		1.000 0.080 4 15778625 missense variant A/G snv 1.2E-05 2.1E-05
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
Secondary malignant neoplasm of colon and/or rectum 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs3756242
rs3756242 		1.000 0.040 4 15784379 intron variant C/A snv 0.15
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		Behavior and Behavior Mechanisms 0.010 1.000 1 2014 2014
dbSNP: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2018 2018
dbSNP: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2018 2018
dbSNP: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C0438696
Disease: Suicidal
Suicidal 		Behavior and Behavior Mechanisms 0.010 1.000 1 2018 2018
dbSNP: rs3796863
rs3796863 		0.790 0.160 4 15848363 intron variant G/T snv 0.41
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs6449182
rs6449182 		0.807 0.160 4 15778830 intron variant C/G snv 0.22
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6449182
rs6449182 		0.807 0.160 4 15778830 intron variant C/G snv 0.22
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6449182
rs6449182 		0.807 0.160 4 15778830 intron variant C/G snv 0.22
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs6449182
rs6449182 		0.807 0.160 4 15778830 intron variant C/G snv 0.22
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
B-CELL MALIGNANCY, LOW-GRADE 		0.010 1.000 1 2009 2009
dbSNP: rs6449182
rs6449182 		0.807 0.160 4 15778830 intron variant C/G snv 0.22
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6449197
rs6449197 		0.882 0.120 4 15813299 intron variant C/T snv 0.23
CUI: C0015458
Disease: Facial Hemiatrophy
Facial Hemiatrophy 		Nervous System Diseases; Stomatognathic Diseases 0.010 1.000 1 2010 2010