Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs72563732
ADIPOQ-AS1 ; ADIPOQ
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs903361
ADORA1
0.882 0.160 1 203122146 intron variant G/A;C snv 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs12447924
CETP
1.000 16 56960280 upstream gene variant C/T snv 0.76 3
rs12597002
CETP
1.000 16 56968492 intron variant C/A snv 0.25 3
rs4674344
CYP27A1
1.000 2 218805152 intron variant A/T snv 0.53 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
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
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
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
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 6
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614