Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs633389 1.000 0.040 11 116796621 upstream gene variant C/T snv 0.13 4
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs1057156731
LMNA
0.925 0.120 1 156137730 missense variant T/A snv 3
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 3
rs2187331
LOC107984343
0.925 0.080 11 68678956 upstream gene variant C/T snv 0.84 3
rs2454727
HCAR2
0.925 0.040 12 122702333 missense variant C/T snv 3
rs3862434
CRTC3
1.000 0.080 15 90537155 intron variant A/G snv 0.48 3
rs59914820
LMNA
0.925 0.160 1 156115000 missense variant C/G;T snv 3
rs7552841
PCSK9
0.925 0.160 1 55053079 intron variant C/T snv 0.32 3
rs774006043
ZPR1 ; APOA5
0.925 0.080 11 116790561 missense variant C/T snv 3
rs9644568 8 20071071 intergenic variant G/A snv 0.11 3
rs972283
LOC105375508
1.000 0.080 7 130782095 intergenic variant A/G;T snv 3
rs11122316
GALNT2
1.000 0.120 1 230101356 intron variant A/G snv 0.42 2
rs11576175
CTSS
1.000 1 150754918 intron variant G/A snv 7.2E-02 2
rs11634397 1.000 0.080 15 80139880 downstream gene variant A/G snv 0.57 2
rs1263163 11 116802796 intergenic variant G/A snv 0.10 2
rs1289389
SLC15A1
13 98684036 3 prime UTR variant C/T snv 0.18 2
rs1335550286
APOE
1.000 0.040 19 44909005 missense variant G/A snv 7.0E-06 2
rs1378577
ABCG1
1.000 0.080 21 42199555 upstream gene variant T/G snv 0.33 2
rs1451659304
LMF1
1.000 0.040 16 868990 missense variant A/C snv 2
rs1468271
LOC107986777 ; NPY
1.000 0.040 7 24287362 intron variant C/T snv 0.97 2
rs1997947
GALNT2
1.000 0.120 1 230148017 intron variant G/A snv 0.78 2
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs2760537
GALNT2
1.000 0.120 1 230190666 intron variant G/A snv 0.23 2
rs2808607
EGLN1
1.000 0.080 1 231405228 intron variant G/A snv 0.56 2