Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15 2
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 3
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 1
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 1
rs10248619
GRB10
7 50683393 intron variant T/C snv 0.71 1
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 2
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs10497870
NBEAL1
2 203105560 intron variant A/C;G snv 1
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10818854
DENND1A
0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 3
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 4
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 3
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs11012732
MLLT10
0.882 0.080 10 21541175 intron variant A/G snv 0.31 1