Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3859192
rs3859192
2 0.925 0.080 17 39972395 intron variant C/T snv 0.42 0.820 1.000 1 2010 2016
dbSNP: rs7212938
rs7212938
2 0.925 0.120 17 39966427 missense variant G/A;C;T snv 4.1E-04; 4.2E-06; 0.52 0.820 0.750 1 2011 2015
dbSNP: rs3894194
rs3894194
3 0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 0.810 1.000 1 2010 2014