Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs6489630
NTF3
0.882 0.080 12 5495458 intron variant T/C snv 0.75 3
rs1884049
ESR1
0.925 0.080 6 151966232 intron variant T/C snv 0.75 2
rs4752293
GRK5
0.882 0.080 10 119342186 intron variant C/T snv 0.74 3
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs2420616
GRK5
0.882 0.080 10 119316984 intron variant A/G snv 0.69 3
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 8
rs2618516
SPON1
0.882 0.080 11 14000092 intron variant T/C snv 0.65 3
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs8126696 0.882 0.080 21 37358422 intron variant T/C snv 0.64 3
rs2337506
CHRNA7
0.925 0.080 15 32053864 intron variant A/G snv 0.60 2
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs8027814
CHRNA7
0.925 0.080 15 32058469 intron variant G/A snv 0.57 2
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs1997794
PDYN-AS1 ; PDYN
0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50 4
rs12976445
SPACA6 ; SPACA6P-AS ; MIRLET7E ; MIR125A
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs2235751
PDYN-AS1 ; PDYN
0.882 0.120 20 1989288 intron variant A/G snv 0.40 3