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: rs104893966
rs104893966
2 0.925 0.160 6 121447428 missense variant A/C snv 0.010 < 0.001 1 2007 2007
dbSNP: rs764670582
rs764670582
5 0.827 0.120 6 121447563 missense variant G/A snv 2.4E-05 4.2E-05 0.010 1.000 1 2013 2013