Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 4
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 3
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 3
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 3
rs12411886
CNNM2
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02 3
rs7660895
SLC2A9
0.882 0.200 4 9983821 intron variant A/G;T snv 3
rs10733376
CDKN2B-AS1
1.000 0.080 9 22114470 intron variant G/C snv 0.64 2
rs727333
DSCAM
1.000 0.080 21 40331020 intron variant C/A snv 6.6E-02 2
rs10958409 1.000 0.080 8 54414531 intergenic variant G/A snv 0.18 1
rs11661542 1.000 0.080 18 22643732 upstream gene variant C/A snv 0.38 1
rs11662668 1.000 0.080 18 22599418 intergenic variant G/A;T snv 0.38 1
rs1504749 1.000 0.080 8 54398151 downstream gene variant A/C snv 0.30 1
rs4800418 1.000 0.080 18 22566777 intergenic variant A/C snv 0.28 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs2280543
BET1L
0.925 0.080 11 203788 3 prime UTR variant C/T snv 4.7E-02 1
rs700651
BOLL
1.000 0.080 2 197766990 intron variant G/A snv 0.73 1
rs6841581
EDNRA
0.882 0.080 4 147480038 upstream gene variant G/A;T snv 1
rs6842241
EDNRA
0.925 0.080 4 147479667 upstream gene variant C/A snv 0.22 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs9864101
IQSEC1
1.000 0.080 3 13148884 intron variant C/T snv 0.58 1
rs383730
LOC107985412
1.000 0.080 1 91416440 intergenic variant C/G;T snv 1