Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11204971
FLG-AS1
0.925 0.120 1 152286602 intron variant A/G snv 0.15 2
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 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
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2
rs1221479287
KIR2DS1 ; KIR3DL1 ; KIR2DL1 ; KIR2DS4
0.925 0.120 19 54783499 missense variant G/A snv 7.0E-06 2
rs1239828657
IL33 ; LOC107987046
0.925 0.120 9 6256028 missense variant T/G snv 4.0E-06 2
rs12568784
FLG2 ; FLG-AS1
0.925 0.120 1 152350656 stop gained G/A;T snv 0.24 0.21 2
rs1335908042
IL37
0.925 0.120 2 112918756 missense variant T/G snv 4.0E-06 2
rs1384974 0.925 0.120 3 177009491 downstream gene variant T/C snv 9.6E-02 2
rs1422985
SPINK5
0.925 0.120 5 148114596 intron variant A/C snv 3.2E-02 2
rs1443712053
FLG-AS1 ; FLG
0.925 0.120 1 152310672 stop gained G/C snv 4.0E-06 2
rs145627745
FLG-AS1 ; FLG
0.925 0.120 1 152313145 missense variant T/A snv 7.8E-03 8.0E-03 2
rs1528473 0.925 0.120 15 55094545 downstream gene variant A/G snv 7.6E-02 2
rs16833974
FLG-AS1 ; FLG2
0.925 0.120 1 152354040 missense variant T/C snv 1.6E-02 6.1E-02 2
rs17718511
SPINK5
0.925 0.120 5 148072009 intron variant A/G snv 3.2E-02 2
rs17718737
SPINK5
0.925 0.120 5 148112898 synonymous variant T/C snv 4.5E-02 3.5E-02 2
rs17860502
SPINK5
0.925 0.120 5 148086438 missense variant G/A snv 4.6E-02 3.2E-02 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
rs2059876
CHST8
0.925 0.120 19 33639430 intron variant C/T snv 0.28 2
rs2066446
IL12RB2
0.925 0.120 1 67315434 intron variant A/G snv 0.20 2
rs2164983 0.925 0.120 19 8679120 downstream gene variant C/A;G snv 0.19 2
rs2228428
CCR4
0.925 0.120 3 32954436 synonymous variant C/T snv 0.25 0.23 2
rs224108 0.925 0.120 10 62789851 intron variant T/C;G snv 0.21 2
rs2303064
SPINK5
0.925 0.120 5 148100517 missense variant G/A snv 0.20 0.25 2