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: rs11683986
rs11683986
2 127438822 intron variant C/T snv 0.28
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.700 1.000 1 2010 2010
dbSNP: rs11683986
rs11683986
2 127438822 intron variant C/T snv 0.28
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
0.700 1.000 1 2010 2010