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: rs55743914
rs55743914 		0.882 0.160 6 127972417 intron variant C/T snv 0.18
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs13197257
rs13197257 		6 128012537 intron variant G/T snv 0.21
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs13197257
rs13197257 		6 128012537 intron variant G/T snv 0.21
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs13200150
rs13200150 		1.000 0.040 6 127988623 intron variant A/G;T snv
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17055223
rs17055223 		6 128023640 intron variant C/A;T snv
CUI: C0678909
Disease: Brain Waves
Brain Waves 		0.700 1.000 1 2018 2018
dbSNP: rs1768353
rs1768353 		0.925 0.040 6 128265251 intron variant G/A snv 6.3E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1768353
rs1768353 		0.925 0.040 6 128265251 intron variant G/A snv 6.3E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3190930
rs3190930 		1.000 0.080 6 127970054 3 prime UTR variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs35469349
rs35469349 		6 127973564 intron variant T/A snv 0.20
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs3933376
rs3933376 		1.000 0.040 6 127970926 intron variant T/A snv 0.14
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs550320694
rs550320694 		6 128238459 intron variant T/C snv 5.9E-04
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2017 2017
dbSNP: rs55743914
rs55743914 		0.882 0.160 6 127972417 intron variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs55743914
rs55743914 		0.882 0.160 6 127972417 intron variant C/T snv 0.18
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6938574
rs6938574 		6 128069835 intron variant T/A;C;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs9321106
rs9321106 		6 128034171 intron variant A/G snv 0.25
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1012049
rs1012049 		6 128209162 intron variant G/A snv 0.44
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1012049
rs1012049 		6 128209162 intron variant G/A snv 0.44
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1339197
rs1339197 		6 128287066 intron variant G/A snv 0.55
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1339197
rs1339197 		6 128287066 intron variant G/A snv 0.55
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs4544930
rs4544930 		6 128073744 intron variant T/C snv 0.83
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs4544930
rs4544930 		6 128073744 intron variant T/C snv 0.83
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs72975913
rs72975913 		1.000 0.120 6 127972787 intron variant C/A snv 0.14
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs72975916
rs72975916 		1.000 0.080 6 127972910 intron variant C/T snv 0.12
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9491896
rs9491896 		1.000 0.080 6 127979804 intron variant G/A snv 8.5E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014