Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs634869 6 139510620 intron variant T/A;C snv 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 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
rs11154370 6 126846446 intron variant A/G;T snv 1
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 1
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 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
rs1406948
UQCC1
20 35317816 intron variant G/A snv 0.44 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 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
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1