Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs7784820
CD36
7 80420717 intron variant A/G snv 0.16 1
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs775077692
CETP
16 56963027 missense variant A/C;G snv 4.0E-06; 4.0E-06 1
rs771561387
VEGFA
1.000 0.080 6 43784557 missense variant C/G;T snv 4.0E-06; 1.2E-05 2
rs770084716
SDCCAG8
1.000 1 243330591 stop gained C/G;T snv 4.0E-06 3
rs770069803
PDE4D
5 58977286 missense variant C/G snv 4.0E-06 1
rs76974938
CFAP298-TCP10L ; CFAP298
1.000 0.080 21 32609946 missense variant C/T snv 1.3E-04 5.5E-04 3
rs76963882
SLC44A5
1.000 0.080 1 75702239 intron variant T/C snv 0.25 2
rs7660268 1.000 0.080 4 14348076 intergenic variant C/A snv 7.4E-02 2
rs762533455
ADRB2
5 148827300 missense variant G/A snv 4.0E-06 1
rs754279998
MKS1
0.776 0.360 17 58208153 inframe deletion GAG/- delins 2.0E-05 1.4E-05 10
rs752977102
APRT
0.925 0.120 16 88811577 missense variant G/C snv 2.8E-05 7.0E-05 3
rs751772105
KCNJ11
11 17387362 missense variant C/A;T snv 4.0E-05 1
rs7456421
HIPK2
0.882 0.120 7 139715976 synonymous variant G/C snv 0.27 0.37 4
rs74183647
LOC107985163 ; NFATC1
18 79396171 5 prime UTR variant G/A;C snv 3
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs73885319
APOL1
0.851 0.120 22 36265860 missense variant A/G snv 1.6E-02 6.6E-02 6
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs730882222
SLC13A5
0.925 0.040 17 6707026 splice donor variant A/C snv 3
rs72881923
LOC105377843
1.000 0.080 6 67286779 intergenic variant T/A;C snv 2
rs72719193
GPHN ; TMEM229B
1.000 0.080 14 67502391 intron variant G/A snv 0.39 2
rs7259572
CERS4
1.000 0.080 19 8226788 intron variant T/A;G snv 2