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: rs10894604
rs10894604 		11 132771851 non coding transcript exon variant T/G snv 0.26
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.800 1.000 1 2013 2013
dbSNP: rs137852691
rs137852691 		0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 3 2008 2013
dbSNP: rs10894670
rs10894670 		11 133352092 intron variant C/A snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2105808
rs2105808 		11 132770106 intron variant A/C snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2221540
rs2221540 		0.925 0.040 11 132846474 intron variant A/G snv 0.11
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs2221540
rs2221540 		0.925 0.040 11 132846474 intron variant A/G snv 0.11
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs2602813
rs2602813 		0.925 0.040 11 133204768 intron variant A/T snv 0.72
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2602813
rs2602813 		0.925 0.040 11 133204768 intron variant A/T snv 0.72
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2917569
rs2917569 		1.000 0.040 11 132698360 intron variant T/C snv 0.51
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs34814382
rs34814382 		11 132831288 intron variant C/A snv 8.9E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4936175
rs4936175 		11 132772064 non coding transcript exon variant T/C snv 0.39
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs55983503
rs55983503 		11 133187586 intron variant A/G snv 0.14
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		Digestive System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7104871
rs7104871 		11 133169304 intron variant T/C snv 0.43
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2015 2015
dbSNP: rs7104890
rs7104890 		11 133331141 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7117082
rs7117082 		0.851 0.080 11 133522399 intron variant G/T snv 0.22
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs7117082
rs7117082 		0.851 0.080 11 133522399 intron variant G/T snv 0.22
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs7117082
rs7117082 		0.851 0.080 11 133522399 intron variant G/T snv 0.22
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		0.700 1.000 1 2014 2014
dbSNP: rs7117082
rs7117082 		0.851 0.080 11 133522399 intron variant G/T snv 0.22
CUI: C3542025
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.700 1.000 1 2014 2014
dbSNP: rs7122854
rs7122854 		1.000 0.040 11 133298628 non coding transcript exon variant A/G snv 0.30
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.700 1.000 1 2012 2012
dbSNP: rs7124348
rs7124348 		11 132515544 intron variant A/G snv 0.23
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs78058594
rs78058594 		11 132410392 downstream gene variant A/G snv 4.1E-02
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7938407
rs7938407 		11 132832593 intron variant C/T snv 8.8E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs137852691
rs137852691 		0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 0
dbSNP: rs1784519
rs1784519 		1.000 0.040 11 132656970 intron variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs3016384
rs3016384 		1.000 0.040 11 132703495 intron variant C/T snv 0.49
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2012 2012