Source: GWASCAT

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: rs2199333
rs2199333
RGS22
0.882 0.040 8 99999120 intron variant C/G;T snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs2199333
rs2199333
RGS22
0.882 0.040 8 99999120 intron variant C/G;T snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2019 2019
dbSNP: rs2199333
rs2199333
RGS22
0.882 0.040 8 99999120 intron variant C/G;T snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2019 2019