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: rs17649553
rs17649553
0.882 0.160 17 45917282 intron variant C/T snv 0.14
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs17649553
rs17649553
0.882 0.160 17 45917282 intron variant C/T snv 0.14
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012