Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 5
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 3
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 3
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 3
rs3765467
GLP1R
1.000 0.080 6 39065819 missense variant G/A;C;T snv 3.6E-02 1.2E-02 3
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 3
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16