Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs11135762 1.000 0.080 8 23633678 downstream gene variant G/A snv 0.65 1
rs9388766
L3MBTL3
0.925 0.080 6 130033710 intron variant T/C snv 0.65 3
rs561104
SELENOF
0.925 0.080 1 86906079 intron variant C/T snv 0.64 2
rs497844 0.925 0.080 5 112849794 intron variant A/G snv 0.64 2
rs1561131
FAR2
0.925 0.080 12 29154998 intron variant G/A snv 0.64 2
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 14
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs2305747
HPN-AS1 ; HPN
0.925 0.080 19 35065453 intron variant C/T snv 0.63 2
rs2305745
HPN-AS1 ; HPN
0.925 0.080 19 35065377 intron variant G/A snv 0.70 0.63 2
rs1270884 0.925 0.080 12 114247766 intergenic variant A/G snv 0.63 2
rs7556371
PIK3C2B
0.925 0.080 1 204488208 intron variant G/A snv 0.62 2
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs746924
TBC1D8 ; RPL31
0.925 0.080 2 101008009 missense variant T/C snv 0.61 0.61 2
rs760317
FHIT
0.925 0.080 3 60113429 intron variant A/G snv 0.60 2
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs41115
APC
0.882 0.160 5 112840073 synonymous variant G/A snv 0.65 0.59 3
rs9889335
CASC17
1.000 0.080 17 71119005 intron variant T/G snv 0.59 1
rs4793529
CASC17
0.925 0.080 17 71122495 intron variant T/C snv 0.59 2
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs6441224
MFSD1 ; RARRES1 ; LOC100287290
0.925 0.080 3 158732628 intron variant T/C snv 0.58 2
rs849140
JAZF1
0.851 0.240 7 28144083 intron variant T/C snv 0.58 7
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs800672
CYP3A43
0.925 0.080 7 99838575 intron variant G/A snv 0.58 2