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: rs11130760
rs11130760 		1.000 0.080 3 60210809 intron variant G/T snv 0.12
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		Neoplasms; Stomatognathic Diseases 0.710 1.000 1 2017 2017
dbSNP: rs2365389
rs2365389 		3 61250788 intron variant C/T snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2018
dbSNP: rs1353545
rs1353545 		1.000 0.040 3 60302116 intron variant G/C snv 0.36
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 4 2015 2019
dbSNP: rs10222378
rs10222378 		1.000 0.040 3 61063307 intron variant A/G;T snv 0.55
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10428174
rs10428174 		3 59828322 intron variant G/A snv 0.72
CUI: C0233849
Disease: Personality Traits
Personality Traits 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs1079196
rs1079196 		3 59821052 intron variant G/A snv 0.22
CUI: C0233849
Disease: Personality Traits
Personality Traits 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs11920657
rs11920657 		0.925 0.040 3 59962844 intron variant G/C snv 4.1E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11920657
rs11920657 		0.925 0.040 3 59962844 intron variant G/C snv 4.1E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs11922368
rs11922368 		3 60882566 intron variant T/C snv 0.61
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs13061562
rs13061562 		1.000 0.040 3 61065916 intron variant T/C snv 0.45
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1353545
rs1353545 		1.000 0.040 3 60302116 intron variant G/C snv 0.36
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs138741635
rs138741635 		0.925 0.040 3 60942161 intron variant T/A;G snv
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs138741635
rs138741635 		0.925 0.040 3 60942161 intron variant T/A;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs139239158
rs139239158 		1.000 0.080 3 59918603 intron variant C/G snv 1.4E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2020 2020
dbSNP: rs141954845
rs141954845 		1.000 0.040 3 61207237 intron variant G/A snv 0.43
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1554600
rs1554600 		1.000 0.080 3 61172101 intron variant G/C snv 1.8E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17257269
rs17257269 		1.000 0.080 3 60039779 intron variant T/C snv 0.15
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs1916799
rs1916799 		3 61247301 intron variant G/A;T snv
CUI: C0005910
Disease: Body Weight
Body Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2017 2017
dbSNP: rs1916799
rs1916799 		3 61247301 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs1916799
rs1916799 		3 61247301 intron variant G/A;T snv
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2017 2017
dbSNP: rs1916801
rs1916801 		3 61201372 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1965143
rs1965143 		1.000 0.040 3 61062993 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1966136
rs1966136 		0.925 0.040 3 61167905 intron variant A/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1966136
rs1966136 		0.925 0.040 3 61167905 intron variant A/C;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs2365389
rs2365389 		3 61250788 intron variant C/T snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017