Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770728618
IL17D
0.925 0.080 13 20721723 missense variant G/C;T snv 5.3E-05 3
rs776933870
PLCE1
0.925 0.080 10 94306632 missense variant A/G snv 8.0E-06 3
rs917870680
MDM2
0.925 0.080 12 68839304 missense variant A/G snv 3
rs121912967
DCC
0.925 0.080 18 52906134 missense variant T/C snv 2
rs3829868
CRNN ; FLG-AS1
0.925 0.080 1 152409644 missense variant C/T snv 0.21 0.15 2
rs41557518
HLA-G
0.925 0.080 6 29828658 frameshift variant C/- delins 2.9E-02 2
rs10437048
PADI4
1.000 0.080 1 17356224 intron variant A/C snv 1
rs10953615 1.000 0.080 7 109512654 intergenic variant A/G snv 0.29 1
rs121918714
TGFBR2
1.000 0.080 3 30691471 missense variant G/C snv 1
rs13294589 1.000 0.080 9 26694890 intergenic variant A/G snv 0.20 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
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs61748181
TERT
0.827 0.120 5 1294051 missense variant C/T snv 2.2E-02 2.2E-02 10
rs17728461
LOC105372988 ; HORMAD2
0.776 0.120 22 30202563 intron variant C/G snv 0.25 9
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs753955
LOC105370113
0.776 0.120 13 23719720 regulatory region variant A/G snv 0.50 9
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs2107301
VDR
0.807 0.120 12 47861787 intron variant G/A snv 0.26 7
rs3176352
CDKN1A
0.807 0.120 6 36684562 intron variant C/A;G;T snv 8.0E-06; 0.37; 2.0E-05 7
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs115510139
COL6A3
0.827 0.120 2 237331726 intron variant A/T snv 0.60 6