Source: CURATED

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
rs1000091588
IGHMBP2
1.000 0.120 11 68935374 stop gained C/T snv 7.0E-06 1
rs1000096
KLF3
4 38691214 intron variant C/T snv 0.39 1
rs10001106 0.925 0.120 4 10125817 intergenic variant T/A;C snv 3
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
rs10001632
CLNK ; LOC105374482
0.925 0.120 4 10520247 intron variant A/C snv 0.97 2
rs10001964
SLC2A9
0.925 0.120 4 9957651 intron variant C/T snv 0.48 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
rs10002268 1.000 0.080 4 55653725 intergenic variant T/C snv 0.41 1
rs10002630
LOC107986195
4 148737523 intron variant G/C snv 0.31 1
rs10002854
SORCS2
1.000 0.040 4 7519419 intron variant C/T snv 8.8E-02 1
rs10002984 0.925 0.120 4 9679109 intron variant T/C snv 0.95 2
rs10003001
SLC2A9
0.925 0.120 4 9982851 intron variant C/T snv 0.21 3
rs10003632
IQCM
4 149563756 missense variant G/T snv 4.1E-02 1
rs10003864 0.925 0.120 4 10435767 downstream gene variant T/C snv 0.29 3
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 1
rs10004892 1.000 0.040 4 188951696 intergenic variant T/C snv 0.21 1
rs10004908 4 87886094 intergenic variant G/A snv 0.70 1
rs10004961
LOC107986195
4 148743746 intron variant C/T snv 0.24 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