Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 1
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs11154370 6 126846446 intron variant A/G;T snv 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 1
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs12731740
MIR29B2CHG
1 207851475 intron variant C/T snv 9.1E-02 1
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 1
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs1406948
UQCC1
20 35317816 intron variant G/A snv 0.44 1
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 1
rs17213965
MYH11
16 15788110 intron variant C/T snv 0.24 1