Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 5
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 2
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 2
rs10994443
ANK3
1.000 0.040 10 60635760 intron variant G/A snv 0.11 2
rs4538475
BST1
1.000 0.040 4 15736314 intron variant A/G snv 0.24 2
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 2
rs12817488
CCDC62
1.000 0.040 12 122811747 intron variant G/A snv 0.39 2
rs9349407
CD2AP
1.000 0.080 6 47485642 intron variant G/C snv 0.23 2
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 2
rs11767557
EPHA1-AS1
0.882 0.080 7 143412046 intron variant T/C snv 0.18 2
rs947211
LOC105371702
0.925 0.040 1 205783537 non coding transcript exon variant A/G snv 0.64 2
rs2814707
LOC112268043 ; C9orf72 ; LOC107987057
0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 2
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 2
rs12734001
PPP1R12B
1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 2
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs6107516
PRNP
1.000 0.120 20 4696446 intron variant G/A snv 0.23 2
rs1994090
SLC2A13
1.000 0.040 12 40034759 intron variant G/A;T snv 2
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 2
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 1
rs6116477 20 4704015 downstream gene variant T/C snv 0.23 1
rs597668
BLOC1S3 ; MARK4
0.925 0.080 19 45205630 intron variant T/A;C;G snv 1
rs1016726
CHN2
7 29316787 intron variant G/A snv 0.12 1