Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4711863
PHACTR1
6 12915185 intron variant G/C snv 0.29 1
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 1
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs565448157
CDKN2B-AS1
9 22029059 intron variant AA/-;A;AAA;AAAA delins 8.0E-04 1
rs616082 18 31787677 intergenic variant C/A;T snv 1
rs7092929
LOC105376360 ; LINC02669
10 3496602 splice region variant A/C;T snv 1
rs712964 22 19168604 upstream gene variant T/C snv 0.66 1
rs7341791
CDKN2B-AS1
9 22112428 intron variant A/G snv 0.65 1
rs741013
PRICKLE2
3 64306961 intron variant A/T snv 6.0E-02 1
rs749924
LINC01880
2 242084344 upstream gene variant C/T snv 0.25 1
rs7857118
CDKN2B-AS1
9 22124141 intron variant A/T snv 0.64 1
rs8089491 18 31763291 upstream gene variant G/A snv 5.4E-02 1
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 4
rs10738604
CDKN2B-AS1
1.000 0.040 9 22025494 intron variant G/A snv 0.29 3
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv 3
rs10811647
CDKN2B-AS1
1.000 0.040 9 22065003 intron variant C/G;T snv 3
rs1004638
CDKN2B-AS1
1.000 0.040 9 22115590 intron variant A/C;T snv 2
rs1008878
CDKN2B-AS1
1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 2
rs10115049
CDKN2B-AS1
1.000 0.040 9 22032120 intron variant A/G snv 0.46 2
rs10217586
CDKN2B-AS1
1.000 0.040 9 22121350 intron variant A/T snv 0.52 2
rs10757264
CDKN2B-AS1
1.000 0.040 9 22019733 intron variant A/G snv 0.58 2
rs10757265
CDKN2B-AS1
1.000 0.040 9 22048860 intron variant T/C snv 0.49 2
rs10757267
CDKN2B-AS1
1.000 0.040 9 22052811 intron variant G/A;C;T snv 2
rs10757270
CDKN2B-AS1
1.000 0.040 9 22072720 intron variant A/C;G snv 0.40 2