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: rs869025608
rs869025608
9 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 2 2014 2016
dbSNP: rs1057519728
rs1057519728
5 0.851 0.120 15 66435103 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519731
rs1057519731
2 0.925 0.040 15 66436816 missense variant G/C snv 0.700 1.000 1 2014 2014
dbSNP: rs1057519856
rs1057519856
2 0.925 0.040 15 66436815 missense variant T/A snv 0.700 1.000 1 2014 2014
dbSNP: rs1057519908
rs1057519908
4 0.882 0.120 15 66435105 missense variant T/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519909
rs1057519909
7 0.790 0.240 15 66435116 missense variant A/C snv 0.700 1.000 1 2016 2016