Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3831317
CHIT1
0.925 0.080 1 203217822 stop gained -/AGACCATGGCCCCGCCCAGTCCCT delins 2
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs2069825
IL6-AS1 ; IL6 ; STEAP1B
1.000 0.040 7 22725718 non coding transcript exon variant -/CC delins 6.7E-05 2
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs121912713
SERPINA1
0.851 0.200 14 94378561 missense variant A/C snv 5
rs3995090
LOC107986462 ; HTR4
1.000 0.040 5 148466252 intron variant A/C snv 0.39 5
rs9554314
FLT1
0.851 0.080 13 28301652 3 prime UTR variant A/C snv 4
rs11852372
HYKK
1.000 0.040 15 78509052 intron variant A/C snv 0.27 3
rs2234694
SOD1
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3
rs57942103
ZFPM2
1.000 0.040 8 105501233 intron variant A/C snv 0.25 3
rs8003379
MTHFD1
0.882 0.160 14 64406881 intron variant A/C snv 0.23 3
rs148133787 1.000 0.040 18 27647495 intergenic variant A/C snv 2.8E-03 2
rs181020201
C1orf185
1.000 0.040 1 51134390 intron variant A/C snv 1.1E-04 2
rs1891385
IL33
0.925 0.120 9 6219845 intron variant A/C snv 0.10 2
rs1912188
SPAG16
1.000 0.040 2 214354143 intron variant A/C snv 0.68 2
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs2293947
EEFSEC
1.000 0.040 3 128378653 intron variant A/C snv 8.4E-02 2
rs4746139
SYNPO2L
1.000 0.040 10 73647891 synonymous variant A/C snv 0.16 0.14 2
rs61781370 1.000 0.040 1 39579628 upstream gene variant A/C snv 0.17 2
rs6677089
CFH
1.000 0.040 1 196715183 intron variant A/C snv 0.46 2
rs7042889 0.925 0.080 9 129033082 upstream gene variant A/C snv 0.15 2
rs11938704
LOC105377462
1.000 0.040 4 144522218 intron variant A/C snv 0.23 1
rs12979270
CYP2B6
1.000 0.040 19 41018226 3 prime UTR variant A/C snv 0.21 1
rs2579762
LRMDA
1.000 0.040 10 76559121 3 prime UTR variant A/C snv 0.39 1