rs9419958, STN1

N. diseases: 5
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.
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.851 0.040 10 103916188 intron variant T/C snv 0.75 0.700 1.000 1 2019 2019
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.851 0.040 10 103916188 intron variant T/C snv 0.75 0.700 1.000 1 2019 2019
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.851 0.040 10 103916188 intron variant T/C snv 0.75 0.700 1.000 1 2019 2019
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.851 0.040 10 103916188 intron variant T/C snv 0.75 0.700 1.000 1 2019 2019
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.851 0.040 10 103916188 intron variant T/C snv 0.75 0.700 1.000 1 2019 2019