Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs3791675
EFEMP1
1.000 0.040 2 55884174 intron variant C/T snv 0.20 4
rs10131
LIG4
1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12 3
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs10494090
SLC25A24
1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs1058319
SLC2A4RG
1.000 0.040 20 63743036 3 prime UTR variant C/A;T snv 0.21 2
rs1064794096
KLLN ; PTEN
1.000 0.040 10 87864514 missense variant A/C;T snv 2
rs10924303
LOC105373265 ; KIF26B
1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs10924690
SMYD3
1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs11163687
LOC107985037
1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs11166389
SLC35A3 ; RNU6-1318P
1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs111696067
GOLGA3
1.000 0.040 12 132799954 intron variant T/C snv 5.3E-04 2
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 2
rs11583706
LOC105373220
1.000 0.040 1 238358337 intron variant G/T snv 0.17 2
rs11598018
STN1
1.000 0.040 10 103901557 intron variant C/A;T snv 2
rs11599775
VTI1A
1.000 0.040 10 112699938 intron variant G/A snv 0.27 2
rs11706832
LRIG1
1.000 0.040 3 66452557 intron variant A/C;G snv 2
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs12125049
LINC02778 ; LOC105378761
1.000 0.040 1 60202030 intergenic variant C/T snv 0.12 2
rs12723208
TRAF5
1.000 0.040 1 211337552 intron variant A/G snv 0.13 2
rs1275600
LOC105369844
1.000 0.040 12 75869771 intron variant T/A snv 0.47 2
rs12803321
PHLDB1
1.000 0.040 11 118609400 intron variant G/C;T snv 2
rs1409785 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 2
rs16838813 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 2