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: rs7006527
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 2 2014 2015
dbSNP: rs7006527
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 2 2014 2015
dbSNP: rs7006527
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 2 2014 2015