Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757277
CDKN2B-AS1
1.000 0.040 9 22124451 intron variant A/G snv 0.40 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 2
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 1
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10847434 1.000 0.040 12 127676248 intergenic variant C/T snv 0.29 1
rs10849917
MYL2
1.000 0.040 12 110919270 intron variant T/A snv 0.13 1
rs10858300 1.000 0.040 9 134950654 intergenic variant C/T snv 0.24 1
rs10923931
NOTCH2
0.925 0.120 1 119975336 intron variant G/T snv 0.17 2
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 1
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs10947460
LOC105375027
1.000 0.040 6 33860457 intergenic variant G/A snv 0.15 1
rs10947463
LINC01016
1.000 0.040 6 33879300 intron variant G/A;T snv 1
rs10953541
BCAP29
1.000 0.040 7 107604100 intron variant C/T snv 0.17 1
rs10980451
SVEP1
1.000 0.040 9 110569988 intron variant C/T snv 1.8E-02 1
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 2
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 1
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 2
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 3
rs11066132
NAA25
1.000 0.040 12 112030402 intron variant C/T snv 5.8E-03 1
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs11067815
LINC02463
1.000 0.040 12 115876463 intron variant A/T snv 0.14 1