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: rs10519177
rs10519177
2 0.925 0.040 15 48464998 intron variant A/G snv 0.35 0.020 0.500 2 2014 2015
dbSNP: rs2118181
rs2118181
6 0.851 0.040 15 48623687 intron variant T/C snv 0.23 0.020 0.500 2 2014 2015
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: rs4774517
rs4774517
3 0.882 0.040 15 48467094 intron variant G/T snv 0.34 0.010 1.000 1 2015 2015
dbSNP: rs755251
rs755251
2 0.925 0.040 15 48519823 intron variant A/G;T snv 0.010 1.000 1 2015 2015
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: rs727503054
rs727503054
15 0.732 0.200 15 48420752 missense variant A/G;T snv 1.6E-05 0.700 0
dbSNP: rs140598
rs140598
5 0.827 0.160 15 48487333 missense variant G/A;C snv 3.2E-02 0.010 1.000 1 1997 1997