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: rs11090598
rs11090598
1 1.000 0.080 22 30125781 intron variant A/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs116895242
rs116895242
1 1.000 0.080 7 124306349 intron variant T/A snv 2.6E-02 0.010 1.000 1 2016 2016
dbSNP: rs12167333
rs12167333
1 1.000 0.080 22 30179823 downstream gene variant C/T snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs12446308
rs12446308
1 1.000 0.080 16 6367932 intron variant A/G snv 8.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs1245371
rs1245371
1 1.000 0.080 6 30070575 3 prime UTR variant A/G snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs1655902
rs1655902
1 1.000 0.080 6 29949078 downstream gene variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs193473
rs193473
1 1.000 0.080 22 30052410 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1978083
rs1978083
1 1.000 0.080 22 30174454 intron variant C/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs200426271
rs200426271
1 1.000 0.080 22 29948468 intron variant -/G ins 0.700 1.000 1 2011 2011
dbSNP: rs2017677
rs2017677
1 1.000 0.080 22 29987273 non coding transcript exon variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2023683
rs2023683
1 1.000 0.080 22 30203607 intron variant G/A snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs2412963
rs2412963
1 1.000 0.080 22 29995292 non coding transcript exon variant G/A snv 0.74 0.700 1.000 1 2011 2011
dbSNP: rs2508049
rs2508049
1 1.000 0.080 6 29856106 intron variant A/G snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs2535238
rs2535238
1 1.000 0.080 6 29677261 5 prime UTR variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2596573
rs2596573
1 1.000 0.080 6 31380153 upstream gene variant C/T snv 0.75 0.700 1.000 1 2011 2011
dbSNP: rs2747457
rs2747457
1 1.000 0.080 6 29688640 intergenic variant T/G snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs28257
rs28257
1 1.000 0.080 22 30033126 intron variant A/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs2956467
rs2956467
1 1.000 0.080 12 48459456 intergenic variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs3129073
rs3129073
1 1.000 0.080 6 29648045 TF binding site variant A/G snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs34978822
rs34978822
1 1.000 0.080 20 63660246 intron variant C/G snv 1.2E-02 0.010 1.000 1 2016 2016
dbSNP: rs36590
rs36590
1 1.000 0.080 22 29932081 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs36594
rs36594
1 1.000 0.080 22 29938393 intron variant C/T snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs36604
rs36604
1 1.000 0.080 22 29944149 intron variant C/A;T snv 0.80 0.700 1.000 1 2011 2011
dbSNP: rs36606
rs36606
1 1.000 0.080 22 29944421 intron variant A/T snv 0.80 0.700 1.000 1 2011 2011
dbSNP: rs36609
rs36609
1 1.000 0.080 22 29948468 intron variant T/G snv 0.74 0.700 1.000 1 2011 2011