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: rs3218020
rs3218020
5 0.882 0.120 9 21997873 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs3217992
rs3217992
22 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 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: rs2069418
rs2069418
2 1.000 0.040 9 22009699 intron variant G/C snv 0.70 0.700 1.000 1 2011 2011
dbSNP: rs2069416
rs2069416
3 0.925 0.040 9 22010005 intron variant T/A;G snv 0.700 1.000 2 2011 2013
dbSNP: rs10811641
rs10811641
2 1.000 0.040 9 22014138 non coding transcript exon variant C/G snv 0.32 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: rs2106119
rs2106119
2 1.000 0.040 9 22017551 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7044859
rs7044859
3 0.925 0.080 9 22018782 intron variant T/A snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs523096
rs523096
7 0.827 0.080 9 22019130 intron variant A/G snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs10757264
rs10757264
2 1.000 0.040 9 22019733 intron variant A/G snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs10965212
rs10965212
3 0.925 0.080 9 22023796 intron variant T/A;C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs496892
rs496892
6 0.827 0.160 9 22024352 intron variant C/T snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10811643
rs10811643
2 1.000 0.040 9 22024967 intron variant A/G snv 0.56 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: rs615552
rs615552
4 0.925 0.120 9 22026078 intron variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs543830
rs543830
2 1.000 0.040 9 22026640 intron variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs7049105
rs7049105
7 0.807 0.120 9 22028802 intron variant A/G snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs188234402
rs188234402
1 9 22029058 intron variant T/A snv 2.1E-05 0.700 1.000 1 2013 2013
dbSNP: rs201049435
rs201049435
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 6.9E-03 0.700 1.000 1 2013 2013
dbSNP: rs34059530
rs34059530
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 0.700 1.000 1 2013 2013
dbSNP: rs397733626
rs397733626
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 0.58 0.700 1.000 1 2013 2013
dbSNP: rs565448157
rs565448157
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 8.0E-04 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: 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