Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 1
rs2226284
LRRC7
1 69869999 intron variant T/C;G snv 0.47 1
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 1
rs2605100
LOC107985272 ; LYPLAL1-AS1
1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 1
rs2820037 1.000 0.040 1 239273242 intergenic variant A/T snv 0.21 1
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 1
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 1
rs659580
PRRX1
1 170664755 intron variant T/C snv 0.81 1
rs7526425 1 211527316 regulatory region variant G/A snv 1
rs876537
CRPP1
1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 1
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs1275988
KCNK3
1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs16849225 2 164050310 intron variant C/T snv 0.19 4
rs1731243
KCNK3
2 26707543 intron variant C/T snv 0.48 4
rs35021474
KCNK3
2 26693976 intron variant C/G snv 0.48 4
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 3
rs6712094 2 164186950 intron variant A/G snv 0.23 3
rs3768939
AGAP1
2 236081413 intron variant G/A snv 0.25 2
rs4665630
KLHL29
0.925 0.080 2 23675447 intron variant C/T snv 0.78 2