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: rs7385804
rs7385804
14 0.851 0.120 7 100638347 intron variant C/A snv 0.65 0.800 1.000 1 2009 2009
dbSNP: rs2075672
rs2075672
8 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs769651870
rs769651870
1 7 100635310 intron variant T/A;C snv 1.2E-03 0.700 1.000 1 2016 2016