Source: GWASDB

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: rs7538876
rs7538876
0.807 0.120 1 17395867 intron variant G/A snv 0.37
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell
0.700 1.000 2 2008 2014
dbSNP: rs7538876
rs7538876
0.807 0.120 1 17395867 intron variant G/A snv 0.37
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010