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: rs671
rs671
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.800 1.000 2 2011 2013
dbSNP: rs10774610
rs10774610
1 1.000 0.040 12 110902439 intron variant T/C snv 0.36 0.800 1.000 1 2011 2011
dbSNP: rs11066280
rs11066280
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.800 1.000 1 2013 2013
dbSNP: rs3782886
rs3782886
22 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 0.700 1.000 2 2011 2013
dbSNP: rs3782889
rs3782889
5 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 0.700 1.000 2 2011 2013
dbSNP: rs10849915
rs10849915
3 0.925 0.080 12 110895818 intron variant T/C snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs11065733
rs11065733
1 1.000 0.040 12 110856716 intron variant A/G snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs11065756
rs11065756
3 0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 0.700 1.000 1 2013 2013
dbSNP: rs11065774
rs11065774
1 1.000 0.040 12 110917522 intron variant G/A snv 4.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs11612727
rs11612727
1 1.000 0.040 12 110876485 intron variant T/C snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs12229654
rs12229654
20 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 0.700 1.000 1 2013 2013
dbSNP: rs2074356
rs2074356
18 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 0.700 1.000 1 2013 2013
dbSNP: rs2157876
rs2157876
1 1.000 0.040 12 111154576 intron variant G/T snv 7.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs2238149
rs2238149
2 1.000 0.040 12 110874125 intron variant T/C snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs3825389
rs3825389
1 1.000 0.040 12 110912967 intron variant C/T snv 7.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs3919447
rs3919447
1 1.000 0.040 12 110953995 intron variant C/T snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs4509829
rs4509829
1 1.000 0.040 12 110958809 non coding transcript exon variant C/T snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs4646776
rs4646776
2 0.925 0.120 12 111792215 intron variant G/A;C snv 1.9E-02 5.8E-03 0.700 1.000 1 2013 2013
dbSNP: rs4766521
rs4766521
1 1.000 0.040 12 110949157 intron variant T/C snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs4766522
rs4766522
1 1.000 0.040 12 110955715 non coding transcript exon variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs4766526
rs4766526
1 1.000 0.040 12 110963512 downstream gene variant G/T snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs4766542
rs4766542
1 1.000 0.040 12 111152688 intron variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs4766549
rs4766549
1 1.000 0.040 12 111180528 intron variant T/G snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs4766553
rs4766553
1 1.000 0.040 12 111196477 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs4766559
rs4766559
1 1.000 0.040 12 111229180 intron variant C/T snv 0.22 0.700 1.000 1 2011 2011