Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2671828 1.000 0.080 17 35404745 upstream gene variant T/C snv 0.55 1
rs3776082 1.000 0.080 5 150164482 upstream gene variant G/A;C snv 1
rs4769585 1.000 0.080 13 27976441 downstream gene variant C/T snv 0.39 1
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1
rs66725070
ALDH1A2
1.000 0.080 15 57975219 intron variant ACAT/- delins 0.35 1
rs717746
CDX1
1.000 0.080 5 150176995 intron variant T/A;C;G snv 1
rs3812863
CDX2
1.000 0.080 13 27971131 upstream gene variant G/A snv 0.48 1
rs150885638
DLG5
1.000 0.080 10 77842176 missense variant T/C snv 6.1E-04 3.5E-04 1
rs9668109
IKBIP
1.000 0.080 12 98617494 intron variant G/A snv 0.15 1
rs2409797
LINC00208
1.000 0.080 8 11576271 non coding transcript exon variant T/C;G snv 1
rs11631094
SLC12A6
1.000 0.080 15 34332237 intron variant G/C;T snv 1
rs3776083
SLC6A7
1.000 0.080 5 150188407 upstream gene variant G/A;C;T snv 1
rs1548445
VPS35L
1.000 0.080 16 19680261 intron variant A/G snv 0.17 1
rs1247942 0.925 0.080 12 114235918 downstream gene variant G/A;C snv 2
rs1979654 0.925 0.080 16 86363229 TF binding site variant G/C snv 0.55 2
rs2687202 0.925 0.080 3 70880832 regulatory region variant T/C snv 0.64 2
rs2701108 0.925 0.160 12 114236456 downstream gene variant T/C snv 0.35 2
rs62423175 0.925 0.080 6 61485463 intergenic variant G/A snv 2
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs491603
AGO3
1.000 0.080 1 36066715 3 prime UTR variant T/A;C snv 2
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs17451754
CFTR
0.925 0.080 7 117616658 intron variant G/A snv 0.10 2
rs199620551
CRTC1
0.925 0.080 19 18693485 intron variant G/- del 9.2E-02 2
rs3072
GDF7
0.925 0.160 2 20678646 3 prime UTR variant T/C snv 0.30 2