rs7006527, RGS22

N. diseases: 4
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 8 100012277 intron variant A/C;T snv 0.700 1.000 2 2014 2015
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.851 0.040 8 100012277 intron variant A/C;T snv 0.700 1.000 2 2014 2015
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.851 0.040 8 100012277 intron variant A/C;T snv 0.700 1.000 2 2014 2015
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.851 0.040 8 100012277 intron variant A/C;T snv 0.700 1.000 1 2014 2014