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
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1805094
LEPR
0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs1805096
LEPR
0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 6
rs2235543
HSD11B1-AS1 ; HSD11B1
0.925 0.080 1 209687323 intron variant T/A;C snv 4
rs4844880
HSD11B1-AS1 ; HSD11B1
0.882 0.240 1 209697571 intron variant A/T snv 0.70 4
rs1057156731
LMNA
0.925 0.120 1 156137730 missense variant T/A snv 3
rs12137855
LYPLAL1
0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs12565406
HSD11B1 ; HSD11B1-AS1
1.000 0.040 1 209687741 intron variant G/A;T snv 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
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs13412852
LPIN1
0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs206833 1.000 0.040 2 31485750 intergenic variant G/A snv 0.17 3
rs62141163 1.000 0.040 2 31440248 regulatory region variant G/A snv 7.6E-02 2
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
rs12373751
ERBB4
1.000 0.040 2 212072166 intron variant T/C snv 0.62 1
rs13428113
LOC107985940 ; INSIG2
1.000 0.040 2 118089309 intron variant T/C snv 0.51 1
rs1881396
ZNF512
1.000 0.040 2 27621734 3 prime UTR variant T/A;G snv 1