Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 5
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 5
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 5
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 4
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 4
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 4
rs17762454
RREB1
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 4
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 4
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 4
rs4665965
MPV17
0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 4
rs780110
IFT172
0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 3
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 3
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3