Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 3
rs6587515 1 150636412 regulatory region variant G/A snv 7.2E-02 2
rs1973993 1 96478438 intergenic variant T/C snv 0.49 1
rs630372 1 177916627 intron variant G/A;T snv 1
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs10198628 2 12824371 intron variant A/G snv 0.59 2
rs577358806
LINC01822
2 21691067 intron variant C/T snv 1.5E-03 2
rs58231626
PAX8 ; PAX8-AS1
2 113256632 non coding transcript exon variant G/A snv 6.8E-04 2
rs13029479 2 655222 regulatory region variant G/A snv 0.13 1
rs6735049 2 630569 intergenic variant T/A;C snv 1
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs9813495
CADM2
3 85777231 intron variant A/G snv 0.15 4
rs1916799
FHIT
3 61247301 intron variant G/A;T snv 3
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 3
rs182381821 3 113643002 intergenic variant T/C snv 3.1E-03 2
rs28721484
PXYLP1 ; ZBTB38
3 141334437 intron variant C/T snv 0.22 2
rs6440919 3 153982187 upstream gene variant C/T snv 0.47 1
rs6780892 3 7947364 downstream gene variant G/A;T snv 1
rs6793368
LOC105374257 ; DGKG
3 186122654 intron variant C/T snv 0.82 1
rs10018902 4 120941346 intergenic variant G/A;T snv 2
rs144582188 4 45163634 intergenic variant CTT/- delins 2
rs112037309
ARHGEF38 ; INTS12
4 105695979 intron variant G/A snv 6.7E-02 1