Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16928973
TRAF6
0.925 0.160 11 36492695 intron variant C/T snv 1.2E-02 2
rs17300593 0.925 0.160 1 58637536 intergenic variant C/G snv 2
rs1942872 0.925 0.160 18 60201132 downstream gene variant C/T snv 0.21 2
rs2796498
PRKAA2
0.925 0.160 1 56678313 intron variant A/G snv 0.47 2
rs2874116 0.925 0.160 18 58792367 regulatory region variant G/A snv 0.36 2
rs2966449
ACTB
0.925 0.160 7 5531994 intron variant C/T snv 0.41 2
rs488846 0.925 0.160 18 54261400 intergenic variant T/C snv 0.26 2
rs499765 0.925 0.160 19 48763133 downstream gene variant C/G snv 0.45 2
rs745452033
SLC12A3
0.925 0.160 16 56865465 missense variant G/C snv 4.0E-06 7.0E-06 2
rs762285755
CUBN
0.925 0.160 10 17114074 missense variant T/C snv 7.6E-05 2.8E-05 2
rs7782979
ELMO1
0.925 0.160 7 36865445 intron variant C/A snv 0.46 2
rs7916840
GPR158
0.925 0.160 10 25424152 intron variant A/T snv 0.70 2
rs9674559
RPTOR
0.925 0.160 17 80741808 intron variant A/G snv 0.22 2
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs994411260
DNMT1
0.925 0.160 19 10194877 missense variant G/C snv 2
rs9958800
PHLPP1 ; LOC105372160
0.925 0.160 18 62773567 intron variant T/A snv 0.25 2
rs9966483
LOC643542
0.925 0.160 18 67783109 intron variant G/A;T snv 2
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 6
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs1056534
FN3K ; TBCD
0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
rs11915160
SOX2 ; SOX2-OT
0.851 0.200 3 181713783 3 prime UTR variant C/A snv 0.11 5