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: rs321986
rs321986
0.882 0.080 7 78668745 intron variant G/A;C;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs321986
rs321986
0.882 0.080 7 78668745 intron variant G/A;C;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs321986
rs321986
0.882 0.080 7 78668745 intron variant G/A;C;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1030015
rs1030015
7 78510264 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs113805659
rs113805659
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
Nutritional and Metabolic Diseases; Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs113805659
rs113805659
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1135402912
rs1135402912
1.000 7 79453250 frameshift variant GGTTCCTG/- delins
CUI: C4539896
Disease: NEPHROTIC SYNDROME, TYPE 15
NEPHROTIC SYNDROME, TYPE 15
0.700 0
dbSNP: rs4727751
rs4727751
1.000 0.040 7 78707618 intron variant T/G snv 0.41
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2015 2015