Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 9
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs12086634
HSD11B1-AS1 ; HSD11B1
0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs6454674
CNR1
0.851 0.120 6 88163211 intron variant T/G snv 0.32 5
rs2280148
SOCS3
0.925 0.080 17 78358299 3 prime UTR variant T/G snv 2.5E-02 2
rs6887452
IL17B
1.000 0.040 5 149404204 upstream gene variant T/G snv 0.32 2
rs1412193981
RHOBTB1
1.000 0.040 10 60877982 missense variant T/G snv 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs7013777 1.000 0.040 8 20020845 intergenic variant T/C;G snv 4
rs879254728
LDLR
0.882 0.080 19 11107511 missense variant T/C;G snv 3
rs3757840
GCK
1.000 0.040 7 44191617 intron variant T/C;G snv 2
rs10085637
LOC107986824 ; PDK4
1.000 0.040 7 95596501 5 prime UTR variant T/C;G snv 0.40 1
rs773837458
SLC2A9
1.000 0.040 4 9834927 missense variant T/C;G snv 8.0E-06 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77