Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs6330
NGF ; NGF-AS1
0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs371237692
REN
0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 5
rs515299
CFH
0.925 0.080 1 196737547 missense variant G/A;C;T snv 4.8E-05; 1.7E-02 4
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 3
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 3
rs770084716
SDCCAG8
1.000 1 243330591 stop gained C/G;T snv 4.0E-06 3
rs12134854
SLC44A5
1.000 0.080 1 75671921 intron variant T/C snv 0.27 2
rs1464816
REN
1.000 0.120 1 204159726 intron variant T/C;G snv 2
rs28415528
THEM4
1.000 0.080 1 151907285 intron variant G/A snv 0.33 2
rs3093058
CRP
1 159715525 upstream gene variant T/A;C;G snv 2
rs6587640
S100A10
1.000 0.080 1 151982754 downstream gene variant C/T snv 0.37 2
rs6657658 1.000 0.080 1 151967388 regulatory region variant T/C snv 0.33 2
rs76963882
SLC44A5
1.000 0.080 1 75702239 intron variant T/C snv 0.25 2
rs17384213
DDAH1
1 85418938 intron variant G/A snv 0.13 1
rs6428106
LOC105371664
1 192585301 intron variant G/T snv 0.14 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34