Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs150016118
UCP3
0.882 0.120 11 74006339 missense variant A/G snv 1.7E-05 6.3E-05 6
rs777659543
UCP3
0.882 0.120 11 74006231 missense variant G/A snv 4.0E-06 6
rs1554483
CLOCK
0.882 0.160 4 55455650 intron variant C/G snv 0.33 5
rs2419621
ACSL5
0.925 0.080 10 112375255 non coding transcript exon variant C/T snv 0.23 3
rs6850524
CLOCK
0.925 0.080 4 55515830 intron variant C/G;T snv 3
rs8450
DENND4B ; CRTC2
1.000 0.040 1 153947810 3 prime UTR variant G/A snv 0.27 2
rs3791783
MSTN ; C2orf88
1.000 0.080 2 190059437 intron variant T/C snv 0.36 2
rs12402521
PDC ; PDC-AS1
1 186453389 intron variant G/A snv 0.33 2