Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10006235
LINC02466
1.000 0.040 4 129748953 non coding transcript exon variant T/C snv 0.73 2
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs10011007 4 130143535 intergenic variant A/C snv 8.3E-02 1
rs10031823 4 102203874 intergenic variant T/C snv 0.68 1
rs1003531
DOT1L
19 2206576 intron variant G/T snv 0.21 1
rs10044158 5 63666886 intergenic variant G/A snv 0.55 1
rs10061788
LINC00461
1.000 0.040 5 88638889 intron variant G/A;T snv 2
rs10070734
LINC00461
5 88644208 intron variant T/A;C snv 1
rs1007934
ZFYVE1
14 72996771 intron variant G/A snv 0.33 3
rs1008078 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 2
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 1
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10133551
AKAP6
14 32813026 intron variant T/C snv 0.30 1
rs10145335
LOC105370655
14 98081411 intron variant G/A snv 0.21 1
rs10147849
AKAP6
14 32835225 3 prime UTR variant T/C snv 0.46 1
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs10165862
LOC105374804
2 73383615 intron variant C/T snv 0.45 1
rs10175405 2 100703250 regulatory region variant G/T snv 0.33 1
rs10182272
CSRNP3
2 165677305 intron variant G/A snv 0.24 1
rs10185725 2 154607197 intergenic variant C/T snv 0.35 1
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs10189912
ARHGAP15
2 143405040 intron variant A/G snv 0.27 1
rs10191758
ARHGAP15
2 143505711 intron variant A/G snv 0.30 1
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10193972
ALMS1
2 73490529 missense variant A/G snv 0.26 0.39 1