Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4704220
CERT1
5 75461731 intron variant G/A snv 0.55 5
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 4
rs731839
PEPD
19 33408159 intron variant G/A snv 0.63 4
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 3
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs13013484 2 27765954 intergenic variant G/A snv 0.61 3
rs5996074
SREBF2
22 41840333 intron variant G/A snv 0.74 3
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3
rs10077823
LOC101929710 ; LOC107986362
5 96510626 intron variant A/G snv 0.43 2
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15 2
rs10173167 2 646767 intergenic variant G/A snv 0.82 2
rs10188334 2 653874 regulatory region variant C/A;T snv 0.15 2
rs10193244 2 647580 intergenic variant T/C snv 0.77 2
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs1026534
LOC101929710 ; LOC107986362
5 96519387 intron variant G/C snv 0.60 2
rs10476682
LOC101929710
5 96522554 intron variant A/G snv 0.38 2
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 2
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs1106683 7 131768766 intergenic variant G/A snv 0.14 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs11231111
AHNAK
11 62492533 intron variant C/T snv 0.15 2
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 2
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 74534327 intron variant -/T delins 2
rs1167800
HIP1
7 75546898 intron variant A/G snv 0.34 2
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 2