Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 14
rs454886
APC
0.763 0.280 5 112810420 intron variant A/G snv 0.26 10
rs281875214
CARD14
0.790 0.160 17 80183976 missense variant A/C snv 7
rs2844484
LTA ; LOC100287329
0.807 0.320 6 31568447 upstream gene variant A/G snv 0.64 6
rs1347671835
IL17C
0.827 0.160 16 88639888 missense variant C/A;G snv 4.3E-06 5
rs199473704
TRPV3
0.882 0.080 17 3524224 missense variant C/A;T snv 5
rs179363865
IKBKG
0.882 0.080 X 154563613 missense variant G/C snv 3
rs375557
LOC105370174
0.882 0.080 13 41557730 intergenic variant G/A;C snv 3
rs1233255
PMS1
1.000 0.040 2 189841366 intron variant A/C snv 0.27 1