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
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs3136534 0.807 0.240 4 122448621 downstream gene variant T/G snv 0.29 6
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 4
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 4
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs6662618 0.882 0.200 1 92469854 downstream gene variant T/G snv 0.75 3
rs2935183
NPEPPS
0.925 0.120 17 47530206 intron variant T/G snv 0.51 2
rs8021741
LOC107984652
0.925 0.160 14 75556057 intergenic variant T/G snv 0.30 2
rs12253981
IL2RA
1.000 0.080 10 6050383 intron variant T/G snv 0.29 1
rs2283792
MAPK1
1.000 0.080 22 21776836 intron variant T/G snv 0.54 1
rs2303759
DKKL1
1.000 0.080 19 49365794 missense variant T/G snv 0.29 0.26 1
rs3095238 1.000 0.080 6 31193433 upstream gene variant T/G snv 0.88 1