Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7732249
PDE4D
1.000 0.040 5 60070442 intron variant C/T snv 0.92 1
rs10750489
NTM
1.000 0.040 11 131786445 intron variant C/G;T snv 0.91 1
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 1
rs4968678
SCN4A ; LOC105371858
1.000 0.040 17 63966848 intron variant A/G snv 0.85 1
rs4234898 1.000 0.040 4 156077389 intergenic variant T/C snv 0.85 1
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 2
rs7550768 1.000 0.040 1 11620226 upstream gene variant C/T snv 0.82 1
rs6782299
LOC101928882 ; CCDC39
0.925 0.080 3 180832914 intron variant G/T snv 0.80 1
rs389883
CYP21A2 ; STK19
0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 4
rs6017203 1.000 0.040 20 43844583 regulatory region variant T/C snv 0.79 1
rs1353920
LOC105377705
1.000 0.040 5 166228848 intergenic variant G/C;T snv 0.79 1
rs1381094 1.000 0.040 3 152755987 intergenic variant C/T snv 0.78 1
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 2
rs1198588 1.000 0.040 1 98087276 intergenic variant A/T snv 0.78 1
rs1538774
SDCCAG8
1.000 0.040 1 243381525 intron variant C/G snv 0.78 1
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 2
rs1530419
PPP2R2B
1.000 0.040 5 146648977 intron variant A/C snv 0.76 1
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 2
rs313327
CHST11
1.000 0.040 12 104580243 intron variant C/T snv 0.75 1
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 1
rs7257304 1.000 0.040 19 15752213 intergenic variant T/C snv 0.71 1
rs1892252
SLC17A4 ; SLC17A1
0.882 0.160 6 25772411 intron variant G/C snv 0.71 3
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3