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: rs1057518809
rs1057518809
4 0.925 0.160 15 48425795 missense variant T/C snv 0.700 0
dbSNP: rs1057518973
rs1057518973
3 0.925 0.120 15 48596343 missense variant A/C;G snv 0.700 0
dbSNP: rs137854466
rs137854466
23 0.724 0.320 15 48411280 stop gained G/A;C snv 4.0E-05; 8.0E-06 0.700 0
dbSNP: rs137854467
rs137854467
7 0.790 0.280 15 48600217 missense variant G/A snv 0.700 0
dbSNP: rs727503057
rs727503057
16 0.708 0.280 15 48505106 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs1036477
rs1036477
5 0.882 0.040 15 48622729 intron variant A/G snv 0.24 0.010 1.000 1 2015 2015
dbSNP: rs2118181
rs2118181
6 0.851 0.040 15 48623687 intron variant T/C snv 0.23 0.010 1.000 1 2015 2015
dbSNP: rs4774517
rs4774517
3 0.882 0.040 15 48467094 intron variant G/T snv 0.34 0.010 1.000 1 2015 2015
dbSNP: rs730880099
rs730880099
11 0.742 0.200 15 48510125 missense variant G/A snv 0.010 1.000 1 2013 2013
dbSNP: rs755251
rs755251
2 0.925 0.040 15 48519823 intron variant A/G;T snv 0.010 1.000 1 2015 2015