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: rs910873
rs910873
PIGU
0.882 0.160 20 34583968 intron variant G/A;C snv
CUI: C0025202
Disease: melanoma
melanoma 		0.810 0.667 1 2008 2017
dbSNP: rs6142206
rs6142206
PIGU
20 34624251 intron variant G/A snv 0.30
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6142206
rs6142206
PIGU
20 34624251 intron variant G/A snv 0.30
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs764598
rs764598
PIGU
20 34573346 intron variant C/G snv 4.7E-02
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs764598
rs764598
PIGU
20 34573346 intron variant C/G snv 4.7E-02
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs910873
rs910873
PIGU
0.882 0.160 20 34583968 intron variant G/A;C snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010