Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs3749474
TMEM165 ; CLOCK
0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs2239704
LTA ; LOC100287329
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs2070673
LOC107984284 ; CYP2E1
0.827 0.160 10 133527063 non coding transcript exon variant A/T snv 0.67 5
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18