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: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.040 1.000 4 2011 2016
dbSNP: rs11030096
rs11030096
3 0.925 0.160 11 27643996 intron variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs11030104
rs11030104
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.010 1.000 1 2016 2016
dbSNP: rs16917204
rs16917204
5 0.827 0.160 11 27646808 intron variant G/C snv 0.17 0.010 1.000 1 2011 2011
dbSNP: rs16917234
rs16917234
2 0.925 0.080 11 27676827 intron variant T/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs7481311
rs7481311
2 0.925 0.160 11 27561582 intron variant T/C snv 0.75 0.010 1.000 1 2016 2016
dbSNP: rs988712
rs988712
2 0.925 0.160 11 27541835 intron variant G/A;T snv 0.010 1.000 1 2016 2016