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: rs1008878
rs1008878
2 1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs2106120
rs2106120
2 1.000 0.040 9 22017102 intron variant G/T snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs10733376
rs10733376
3 1.000 0.080 9 22114470 intron variant G/C snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.800 1.000 2 2011 2013
dbSNP: rs2069418
rs2069418
2 1.000 0.040 9 22009699 intron variant G/C snv 0.70 0.700 1.000 1 2011 2011
dbSNP: rs7865618
rs7865618
11 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.700 1.000 2 2011 2013
dbSNP: rs1063192
rs1063192
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1537372
rs1537372
14 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs679038
rs679038
2 1.000 0.040 9 22029081 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1333039
rs1333039
2 1.000 0.040 9 22065658 splice region variant G/A;C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs8181050
rs8181050
2 1.000 0.040 9 22064392 intron variant G/A;C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10757267
rs10757267
2 1.000 0.040 9 22052811 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10811651
rs10811651
2 1.000 0.040 9 22067831 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs1556516
rs1556516
1 9 22100177 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs944801
rs944801
4 0.882 0.120 9 22051671 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs9632884
rs9632884
6 0.851 0.160 9 22072302 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs3218020
rs3218020
5 0.882 0.120 9 21997873 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs4977756
rs4977756
24 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs10120688
rs10120688
7 0.807 0.080 9 22056500 intron variant G/A snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs10738604
rs10738604
3 1.000 0.040 9 22025494 intron variant G/A snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs10811645
rs10811645
2 1.000 0.040 9 22049657 intron variant G/A snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs10965215
rs10965215
4 0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 0.700 1.000 1 2013 2013
dbSNP: rs7028268
rs7028268
2 1.000 0.040 9 22048415 intron variant G/A snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs7028570
rs7028570
2 1.000 0.040 9 22048684 intron variant G/A snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs9632885
rs9632885
2 1.000 0.040 9 22072639 intron variant G/A snv 0.56 0.700 1.000 1 2013 2013