Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10953615 1.000 0.080 7 109512654 intergenic variant A/G snv 0.29 1
rs13294589 1.000 0.080 9 26694890 intergenic variant A/G snv 0.20 1
rs10437048
PADI4
1.000 0.080 1 17356224 intron variant A/C snv 1
rs2477134
PADI4
1.000 0.080 1 17307077 upstream gene variant G/A;T snv 1
rs2501796
PADI4
1.000 0.080 1 17307027 upstream gene variant G/A;C snv 1
rs41265997
PADI4
1.000 0.080 1 17342111 missense variant C/G;T snv 4.0E-06; 1.6E-05 1
rs4924935
PRPSAP2
1.000 0.080 17 18850557 intron variant C/G;T snv 1
rs121918714
TGFBR2
1.000 0.080 3 30691471 missense variant G/C snv 1
rs3829868
CRNN ; FLG-AS1
0.925 0.080 1 152409644 missense variant C/T snv 0.21 0.15 2
rs121912967
DCC
0.925 0.080 18 52906134 missense variant T/C snv 2
rs41557518
HLA-G
0.925 0.080 6 29828658 frameshift variant C/- delins 2.9E-02 2
rs10088262
LOC105375739
0.925 0.160 8 123753462 intergenic variant A/G snv 0.56 2
rs312986 0.925 0.080 18 1898710 intron variant A/G;T snv 3
rs11125529
ACYP2
0.882 0.280 2 54248729 intron variant C/A;T snv 3
rs7436
COL6A3
0.925 0.080 2 237324168 3 prime UTR variant T/A snv 0.10 3
rs750408412
CYP2E1
0.925 0.080 10 133538938 missense variant A/G snv 3
rs1014867
FAT4
0.925 0.080 4 125491736 missense variant C/T snv 4.9E-02 4.9E-02 3
rs1039808
FAT4
0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 3
rs12508222
FAT4
0.925 0.080 4 125449492 missense variant G/A;T snv 4.3E-02; 2.0E-05 3
rs1567047
FAT4
0.925 0.080 4 125451587 missense variant G/A snv 0.27 0.22 3
rs753225272
FAT4
0.925 0.080 4 125491730 missense variant C/G;T snv 8.0E-06; 4.0E-06 3
rs1057519900
FGFR2
0.882 0.120 10 121515259 missense variant C/T snv 3
rs770728618
IL17D
0.925 0.080 13 20721723 missense variant G/C;T snv 5.3E-05 3
rs31564
IL9
0.925 0.080 5 135894564 intron variant G/A;T snv 3
rs4269383
LOC105378072 ; LOC101928923
0.882 0.120 6 155876368 intergenic variant A/G snv 0.37 3