Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs115746363
FLG-AS1 ; FLG
0.882 0.120 1 152312410 stop gained G/A;C snv 6.0E-04 3
rs13139310
IRF2
0.925 0.120 4 184435757 intron variant G/A;C snv 3
rs149484917
FLG-AS1 ; FLG
0.882 0.120 1 152304939 stop gained G/C;T snv 4.7E-04; 4.0E-06 3
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 3
rs2303070
SPINK5
0.882 0.120 5 148120328 missense variant G/A;C;T snv 0.13 3
rs360721
IL18
0.882 0.200 11 112155193 intron variant G/A;C snv 3
rs438421
IL12RB1
0.882 0.200 19 18065276 intron variant A/G;T snv 3
rs7124842 0.882 0.160 11 76600576 intergenic variant G/A;C;T snv 3
rs761212672
FLG-AS1 ; FLG
0.882 0.120 1 152304999 stop gained G/T snv 3.2E-05 3
rs9290927
LOC107986170
0.882 0.120 3 190304727 downstream gene variant A/G;T snv 3
rs11150780
SLC38A10
0.925 0.120 17 81290360 intron variant A/G;T snv 2
rs113136594
FLG ; FLG-AS1
0.925 0.120 1 152313436 missense variant G/A;C;T snv 6.0E-04; 4.0E-06; 8.0E-06 2
rs1239828657
IL33 ; LOC107987046
0.925 0.120 9 6256028 missense variant T/G snv 4.0E-06 2
rs1335908042
IL37
0.925 0.120 2 112918756 missense variant T/G snv 4.0E-06 2
rs1443712053
FLG-AS1 ; FLG
0.925 0.120 1 152310672 stop gained G/C snv 4.0E-06 2
rs180768115
FLG-AS1 ; FLG
0.925 0.120 1 152310342 stop gained G/C;T snv 8.0E-06; 1.7E-04 2
rs199720399
NLN
0.925 0.120 5 65792557 missense variant T/C snv 2
rs28441202
RPTN ; PUDPP2
0.925 0.120 1 152156387 missense variant A/G snv 2
rs2897442
KIF3A
0.925 0.120 5 132713335 intron variant C/A;T snv 2
rs380743
RASIP1
0.925 0.120 19 48737757 intron variant G/A;C snv 2
rs4705962
KIF3A
0.925 0.160 5 132693166 3 prime UTR variant T/A;C snv 2
rs560912365
FLG ; FLG-AS1
0.925 0.120 1 152309046 stop gained C/G;T snv 4.0E-06; 2.2E-04 2
rs5743409
DEFB1
0.925 0.120 8 6879098 intron variant C/A;G snv 2
rs612529
VSTM1
0.925 0.120 19 54063999 upstream gene variant A/G;T snv 2