Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 5
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 5
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs12447924
CETP
1.000 16 56960280 upstream gene variant C/T snv 0.76 3
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
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs7946
PEMT
0.851 0.160 17 17506246 missense variant C/T snv 0.59 0.59 6
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs4674344
CYP27A1
1.000 2 218805152 intron variant A/T snv 0.53 1
rs6006469
SAMM50
1.000 22 43987737 non coding transcript exon variant C/G snv 0.49 1
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs2235778
SAMM50
1.000 22 43993634 intron variant T/C snv 0.48 1
rs3788604
SAMM50
1.000 22 43992537 intron variant A/G snv 0.48 1
rs6006468
SAMM50
1.000 22 43987552 non coding transcript exon variant G/C snv 0.48 1
rs6006602
SAMM50
1.000 22 43987520 non coding transcript exon variant C/T snv 0.48 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2281292
SAMM50 ; PARVB
1.000 22 43999509 intron variant A/C snv 0.44 0.47 1
rs6006473
PARVB ; SAMM50
0.925 0.040 22 43997195 intron variant C/T snv 0.47 2
rs4823182
SAMM50
0.925 0.080 22 43981562 intron variant A/G snv 0.46 2
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 6