Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4849133 2 112923864 downstream gene variant C/A;T snv 2
rs757533393
POFUT1
1.000 20 32216664 missense variant C/G;T snv 1.2E-05 2
rs1281032650
LNPEP
5 96979168 missense variant A/G snv 1
rs1290547844
BRD4
19 15273041 missense variant C/T snv 4.0E-06 1
rs1316569885
SORBS1
10 95399139 missense variant C/T snv 4.0E-06 7.0E-06 1
rs1325863623
SERPINB6
6 2953175 missense variant C/T snv 4.0E-06 1
rs1921
ISG15
1 1014228 missense variant G/A;C snv 0.36 1
rs200192581
SORBS1
10 95381729 missense variant C/T snv 8.0E-06 7.0E-06 1
rs2071025
COL11A2
6 33175979 intron variant A/G snv 0.28 0.29 1
rs3116996 6 33130187 downstream gene variant T/A snv 0.13 1
rs7314777
LOC105369818
12 68256855 upstream gene variant T/C snv 0.19 1
rs751703423
AIMP2 ; EIF2AK1
7 6023410 missense variant G/A;C snv 1
rs778438430
SORBS1
10 95381747 missense variant C/T snv 1.6E-05 2.8E-05 1
rs779770523
SORBS1
10 95432543 missense variant C/G;T snv 1.2E-05; 4.0E-06 1
rs781314841
SORBS1
10 95341566 missense variant C/T snv 4.4E-05 2.8E-05 1
rs868564661
FGFR2
10 121487415 missense variant G/A snv 1
rs954917585
FGFR2
10 121479973 missense variant G/A snv 8.0E-06 1.4E-05 1
rs2294918
PNPLA3
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs35724
NR1H4
0.925 0.040 12 100561600 intron variant C/G snv 0.52 3
rs1371149614
SHBG
1.000 0.040 17 7630488 missense variant G/C snv 4.0E-06 2
rs1051861187
ABCB4
0.827 0.080 7 87409385 missense variant A/G snv 6
rs57749775
KRT8
0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs80338707
LOC100130283 ; PMM2
0.925 0.080 16 8847775 missense variant G/A;C snv 6.8E-05; 4.0E-06 4
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3