Source: ALL
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: rs1004638
rs1004638
CDKN2B-AS1
3 1.000 0.040 9 22115590 intron variant A/C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs1008878
rs1008878
CDKN2B-AS1
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: rs10115049
rs10115049
CDKN2B-AS1
2 1.000 0.040 9 22032120 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs10116277
rs10116277
CDKN2B-AS1
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.700 1.000 2 2011 2013
dbSNP: rs10120688
rs10120688
CDKN2B-AS1
7 0.807 0.080 9 22056500 intron variant G/A snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs10127775
rs10127775
GALNT2
4 1 230160042 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10211524
rs10211524
LINC02245 ; LOC107984063
4 2 64980940 intron variant G/A snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs10217586
rs10217586
CDKN2B-AS1
2 1.000 0.040 9 22121350 intron variant A/T snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10500569
rs10500569
LOC107984814
1 16 72722202 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10502575
rs10502575 		1 18 31756628 downstream gene variant A/G snv 6.9E-02 0.800 1.000 1 2013 2013
dbSNP: rs10511701
rs10511701
CDKN2B-AS1
2 9 22112600 intron variant T/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs1063192
rs1063192
CDKN2B ; CDKN2B-AS1
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10733376
rs10733376
CDKN2B-AS1
3 1.000 0.080 9 22114470 intron variant G/C snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs10738604
rs10738604
CDKN2B-AS1
3 1.000 0.040 9 22025494 intron variant G/A snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs10738605
rs10738605
CDKN2B-AS1
3 0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10738606
rs10738606
CDKN2B-AS1
2 1.000 0.040 9 22088091 intron variant A/T snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs10738607
rs10738607
CDKN2B-AS1
4 0.925 0.080 9 22088095 intron variant A/G snv 0.42 0.700 1.000 2 2011 2013
dbSNP: rs10738609
rs10738609
CDKN2B-AS1
3 1.000 0.040 9 22114496 intron variant A/C;G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10738610
rs10738610
CDKN2B-AS1
5 0.882 0.120 9 22123767 intron variant A/C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10757264
rs10757264
CDKN2B-AS1
2 1.000 0.040 9 22019733 intron variant A/G snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs10757265
rs10757265
CDKN2B-AS1
2 1.000 0.040 9 22048860 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs10757267
rs10757267
CDKN2B-AS1
2 1.000 0.040 9 22052811 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10757269
rs10757269
CDKN2B-AS1
4 1.000 0.040 9 22072265 intron variant A/C;G snv 0.700 1.000 2 2011 2013
dbSNP: rs10757270
rs10757270
CDKN2B-AS1
2 1.000 0.040 9 22072720 intron variant A/C;G snv 0.40 0.700 1.000 1 2013 2013