Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs1199047
CCDC88B
0.882 11 64350711 intron variant A/C snv 0.38 4
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs12980063
CPT1C
0.882 19 49693735 intron variant A/G snv 0.48 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs13299616
PSMD5 ; CUTALP
0.882 9 120832525 intron variant T/C snv 0.50 4
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4
rs142647938
KCNH7
0.882 2 162516642 intron variant C/A;T snv 4
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 5
rs145268310 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 4
rs1530687
ARHGAP31
0.882 3 119395668 intron variant G/A snv 0.46 4
rs1534430
MIR3681HG
0.851 0.040 2 12504610 intron variant C/T snv 0.35 5
rs1549922 0.882 5 159304540 intergenic variant G/A snv 0.56 4
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs1790588
CD226
0.882 18 69867948 intron variant T/C snv 0.55 4
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4