Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs391300
SRR
0.882 0.160 17 2312964 intron variant T/C snv 0.58 4
rs59007384
TOMM40
0.851 0.080 19 44893408 intron variant G/A;T snv 4
rs12344615
UBQLN1
0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 4
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 3
rs1207568
KL
0.925 0.120 13 33016046 upstream gene variant G/A snv 0.17 3
rs1859788
PILRA
0.925 0.080 7 100374211 missense variant A/C;G snv 4.0E-06; 0.65 3
rs3796529
REST
0.925 0.080 4 56931248 missense variant C/T snv 0.22 0.22 3
rs1010159
SORL1
0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 3
rs1784933
SORL1
0.882 0.080 11 121618707 intron variant G/A snv 0.84 3
rs641120
SORL1
0.882 0.080 11 121510256 intron variant G/A snv 0.38 3
rs157581
TOMM40
0.925 0.080 19 44892457 synonymous variant T/C snv 0.25 0.29 3
rs3747742
TREML2
0.882 0.080 6 41194780 missense variant T/C snv 0.33 0.29 3
rs4718789 0.925 0.120 7 68579188 intergenic variant C/T snv 8.1E-02 2
rs1451603364
BDNF-AS ; BDNF
0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06 2
rs3756577
CAMK2A
0.925 0.080 5 150249081 intron variant C/T snv 0.14 2
rs3822606
CAMK2A
0.925 0.080 5 150261592 intron variant G/A snv 0.27 2
rs6598008
CDHR5
0.925 0.080 11 618172 intron variant A/G snv 0.48 2
rs4837766
CDK5RAP2
0.925 0.080 9 120402006 intron variant A/C;G;T snv 2
rs111943087
CSF1R
0.925 0.080 5 150059725 missense variant G/A snv 1.4E-05 2
rs9340803
ESR1
0.925 0.080 6 151842832 intron variant A/G snv 1.0E-03 3.8E-04 2
rs35445101
HLA-DRB1
0.925 0.080 6 32579102 missense variant A/G snv 4.2E-04 2.7E-02 2
rs12053868
IL1RAP
0.925 0.080 3 190582215 intron variant A/G snv 8.0E-02 2
rs6850306
LCORL
0.925 0.080 4 18004466 intron variant G/A snv 0.12 2