Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10876864
IKZF4
0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50 4
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 4
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 4
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51 4
rs61754230
RAB21
12 71785666 missense variant C/T snv 1.3E-02 1.2E-02 4
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs10774547 0.925 0.120 12 120424913 intergenic variant T/C snv 0.39 3
rs1541374 4 105127203 intergenic variant T/A;G snv 3
rs2008514 16 28814284 non coding transcript exon variant G/A snv 0.35 3
rs28600726 1.000 0.040 4 158730723 intergenic variant G/A snv 0.53 3
rs3843954 1.000 0.040 13 57974377 intergenic variant G/A;C snv 3
rs475616 10 30207976 regulatory region variant A/G snv 0.67 3
rs55771711 1.000 0.040 10 131989233 intergenic variant G/C snv 0.24 3
rs61572747 1.000 0.040 17 45383525 regulatory region variant A/G snv 0.25 3
rs6940116 1.000 0.040 6 27740953 upstream gene variant A/G snv 0.18 3
rs7613360 1.000 0.040 3 49879277 upstream gene variant C/T snv 0.32 3
rs901630 6 98091643 intron variant C/T snv 0.32 3
rs11688767
ACTG1P22
0.925 0.040 2 57761059 intron variant A/T snv 0.40 3
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 3