rs7907606, None

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 2 2018 2019
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 2 2018 2019
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 1 2016 2016
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 1 2016 2016
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.010 1.000 1 2018 2018
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.010 1.000 1 2018 2018