Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs9415705
JMJD1C
1.000 0.120 10 63401790 intron variant T/G snv 0.13 1
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2893922
JMJD1C
1.000 0.120 10 63487259 intron variant T/C;G snv 1
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs1003706636
NLRP3
1.000 0.120 1 247424639 missense variant T/C snv 1
rs10128264
ZMIZ1
1.000 0.120 10 79200216 intron variant T/C snv 0.64 1
rs10956445
CCDC26
1.000 0.120 8 128775730 intron variant T/C snv 0.20 1
rs11817689 1.000 0.120 10 63164457 downstream gene variant T/C snv 0.13 1
rs9415699
JMJD1C
1.000 0.120 10 63383798 intron variant T/C snv 0.13 1
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14