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: rs1051794
rs1051794
5 0.925 0.120 6 31411332 missense variant G/A snv 0.34 0.35 0.700 1.000 1 2009 2009
dbSNP: rs2256175
rs2256175
5 1.000 6 31412672 intron variant C/T snv 0.55 0.700 1.000 1 2009 2009
dbSNP: rs2596542
rs2596542
18 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs59440261
rs59440261
5 0.925 6 31403294 intron variant C/A snv 3.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs6910087
rs6910087
4 1.000 6 31409270 intron variant C/T snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs9266825
rs9266825
4 1.000 6 31415105 3 prime UTR variant C/A;T snv 0.31; 8.1E-06 0.700 1.000 1 2009 2009