Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000005
LINC00945
21 33060745 intron variant G/C snv 0.51 1
rs10000770
INPP4B
1.000 0.040 4 142693109 intron variant C/T snv 0.11 1
rs1000096
KLF3
4 38691214 intron variant C/T snv 0.39 1
rs1000113
IRGM
0.925 0.040 5 150860514 intron variant C/T snv 0.13 1
rs10001414
PALLD
1.000 0.040 4 168569930 intron variant A/G snv 1.7E-02 1
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs10002082
MARCHF1
4 164159753 intron variant A/G snv 0.20 1
rs10002111
LOC105377262
4 66949786 regulatory region variant A/G snv 0.82 1
rs10002854
SORCS2
1.000 0.040 4 7519419 intron variant C/T snv 8.8E-02 1
rs10004892 1.000 0.040 4 188951696 intergenic variant T/C snv 0.21 1
rs10005067 4 87931491 intergenic variant T/A;C snv 1
rs10005233
SNCA
1.000 0.040 4 89822180 3 prime UTR variant C/T snv 0.58 0.59 1
rs10005540 4 173660916 downstream gene variant C/G;T snv 1
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs1000597 0.925 0.120 7 30897563 intron variant T/A;C snv 2
rs10006108 1.000 0.040 4 97002862 intergenic variant C/T snv 0.48 1
rs10006235
LINC02466
1.000 0.040 4 129748953 non coding transcript exon variant T/C snv 0.73 2
rs10006237 4 136606920 intergenic variant C/T snv 0.50 1
rs10006327
SLC9B1
1.000 0.080 4 102969823 intron variant T/A;C snv 1
rs10006418
INPP4B
1.000 0.040 4 142691588 intron variant A/T snv 0.11 1
rs10007052
RNF150
1.000 0.040 4 141084419 intron variant C/A snv 0.31 1
rs1000708
SLC16A7
1.000 0.160 12 59689707 intron variant C/T snv 0.58 1
rs10007186
LINC01094
4 78667891 intron variant C/T snv 0.65 1
rs1000791
RBFOX3
17 79269796 intron variant T/A snv 8.2E-02 1
rs10007975
C4orf17
4 99527667 intron variant C/T snv 0.27 1