Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs188845491
rs188845491
CYP3A7 ; CYP3A51P ; ZSCAN25 ; CYP3A7-CYP3A51P
1.000 0.040 7 99689016 intron variant C/T snv 2.5E-04
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.700 1.000 1 2015 2015
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10211
rs10211
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
1.000 0.080 7 99705371 3 prime UTR variant T/C snv 0.25
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs28451617
rs28451617
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.851 0.120 7 99735142 5 prime UTR variant C/T snv 9.2E-03 3.3E-02
CUI: C1841972
Disease: Glucocorticoid Receptor Deficiency
Glucocorticoid Receptor Deficiency 		0.010 1.000 1 2012 2012
dbSNP: rs28451617
rs28451617
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.851 0.120 7 99735142 5 prime UTR variant C/T snv 9.2E-03 3.3E-02
CUI: C0035220
Disease: Respiratory Distress Syndrome, Newborn
Respiratory Distress Syndrome, Newborn 		0.010 1.000 1 2012 2012
dbSNP: rs28451617
rs28451617
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.851 0.120 7 99735142 5 prime UTR variant C/T snv 9.2E-03 3.3E-02
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Adult 		0.010 1.000 1 2012 2012
dbSNP: rs28451617
rs28451617
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.851 0.120 7 99735142 5 prime UTR variant C/T snv 9.2E-03 3.3E-02
CUI: C0852283
Disease: Respiratory Distress Syndrome
Respiratory Distress Syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2016 2016
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2016 2016
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C1740827
Disease: CLL progression
CLL progression 		0.010 1.000 1 2016 2016
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2016 2016
dbSNP: rs45446698
rs45446698
CYP3A7 ; ZSCAN25 ; CYP3A7-CYP3A51P
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2016 2016