Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv 9
rs10392
PPP1R16B
0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs113857788
CFTR
0.882 0.160 7 117664780 missense variant G/C;T snv 1.0E-03; 6.0E-05 5
rs12688220
MORC4
0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 5
rs7057398
MORC4 ; RIPPLY1 ; CLDN2
0.827 0.080 X 106901299 intron variant T/C snv 0.41 5
rs6622126
MORC4
0.851 0.080 X 106956972 missense variant G/A snv 0.58 4
rs1800907 0.925 0.120 7 142800425 upstream gene variant T/C snv 0.56 3
rs12014762
MORC4
0.882 0.080 X 106940440 intron variant C/T snv 0.14 3
rs12008279
MORC4 ; CLDN2
0.882 0.080 X 106917472 intron variant A/G;T snv 3
rs17251
TRBV27
0.925 0.120 7 142715462 intron variant C/A snv 0.33 0.37 3
rs59536457
KRT8
0.925 0.080 12 52904795 missense variant T/C snv 4.1E-03 3.1E-03 2
rs768255958
PRSS1
0.925 0.080 7 142751805 missense variant A/G snv 4.0E-06 2
rs10243591 1.000 0.080 7 142725721 downstream gene variant C/A;T snv 1
rs10465287 1.000 0.080 X 106545130 intergenic variant T/A;G snv 1
rs12857658 1.000 0.080 X 107281285 intergenic variant G/A snv 5.0E-02 1
rs1298993 1.000 0.080 X 107043226 regulatory region variant G/A snv 0.18 1
rs13239736 1.000 0.080 7 142620329 downstream gene variant G/T snv 0.71 1
rs138520829 1.000 0.080 X 106504267 intergenic variant T/C snv 5.4E-02 1
rs144184641 1.000 0.080 7 142775173 downstream gene variant T/A;C snv 1
rs146437551 1.000 0.080 5 147808460 intergenic variant T/G snv 8.8E-03 1
rs148771016 1.000 0.080 X 107318205 intergenic variant A/C snv 5.1E-02 1
rs148933117 1.000 0.080 1 15791573 upstream gene variant A/C snv 3.3E-02 1