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: rs11655081
rs11655081
7 0.851 0.080 17 68386068 intron variant T/C snv 0.18 0.010 1.000 1 2014 2014
dbSNP: rs1182
rs1182
9 0.790 0.160 9 129813781 3 prime UTR variant C/A snv 0.17 0.010 1.000 1 2015 2015
dbSNP: rs1265889947
rs1265889947
1 1.000 0.040 2 178450382 missense variant C/G snv 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs3842225
rs3842225
6 0.882 0.120 9 129813148 3 prime UTR variant C/- del 0.16 0.010 1.000 1 2015 2015
dbSNP: rs587776983
rs587776983
9 0.807 0.240 19 6502209 missense variant G/A;C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs886041099
rs886041099
1 1.000 0.040 9 129818784 missense variant T/A snv 0.010 1.000 1 2014 2014
dbSNP: rs1801968
rs1801968
7 0.827 0.040 9 129818622 missense variant C/G;T snv 0.13; 4.0E-06 0.010 < 0.001 1 2010 2010
dbSNP: rs587777074
rs587777074
7 0.790 0.240 19 6495688 missense variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs767114942
rs767114942
1 1.000 0.040 9 129818826 missense variant A/G snv 1.2E-05 1.4E-05 0.010 1.000 1 2014 2014