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: rs543830
rs543830
2 1.000 0.040 9 22026640 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs568447
rs568447
1 1.000 0.040 9 22021616 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs613312
rs613312
1 1.000 0.040 9 22026595 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs679038
rs679038
2 1.000 0.040 9 22029081 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7027048
rs7027048
2 1.000 0.040 9 22053710 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8181050
rs8181050
2 1.000 0.040 9 22064392 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9632884
rs9632884
6 0.851 0.160 9 22072302 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs572101477
rs572101477
1 1.000 0.040 9 21999330 intron variant GTTAT/- delins 9.8E-04 0.700 1.000 1 2012 2012
dbSNP: rs1412830
rs1412830
1 1.000 0.040 9 22043613 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs573687
rs573687
3 0.882 0.120 9 22011643 intron variant G/A snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs2811713
rs2811713
1 1.000 0.040 9 21999329 intron variant G/A snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs581876
rs581876
1 1.000 0.040 9 22022377 intron variant C/T snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs597816
rs597816
1 1.000 0.040 9 22021173 intron variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs599452
rs599452
1 1.000 0.040 9 22027403 intron variant G/A snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs634537
rs634537
6 0.851 0.080 9 22032153 intron variant T/G snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1412829
rs1412829
14 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs564398
rs564398
18 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 0.700 1.000 2 2012 2012
dbSNP: rs10738604
rs10738604
3 1.000 0.040 9 22025494 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs615552
rs615552
4 0.925 0.120 9 22026078 intron variant T/C snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs518394
rs518394
6 0.827 0.160 9 22019674 intron variant G/C snv 0.30 0.700 1.000 2 2012 2012
dbSNP: rs523096
rs523096
7 0.827 0.080 9 22019130 intron variant A/G snv 0.30 0.710 1.000 3 2012 2012
dbSNP: rs3217992
rs3217992
22 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 0.700 1.000 1 2012 2012
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 2012 2012
dbSNP: rs7028268
rs7028268
2 1.000 0.040 9 22048415 intron variant G/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs10811650
rs10811650
5 0.882 0.200 9 22067594 intron variant A/G snv 0.37 0.700 1.000 1 2012 2012