Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759188048
MSRA
8 10066778 intron variant G/A;T snv 1
rs112037309
ARHGEF38 ; INTS12
4 105695979 intron variant G/A snv 6.7E-02 1
rs494558
COL4A1
13 110276815 intron variant C/T snv 0.90 2
rs58231626
PAX8 ; PAX8-AS1
2 113256632 non coding transcript exon variant G/A snv 6.8E-04 2
rs182381821 3 113643002 intergenic variant T/C snv 3.1E-03 2
rs12705992 7 114789947 regulatory region variant G/A snv 0.72 1
rs10782199
LOC105377975
6 119791894 intergenic variant G/A snv 0.32 1
rs9374842 6 119864519 regulatory region variant C/T snv 0.76 2
rs10018902 4 120941346 intergenic variant G/A;T snv 2
rs10198628 2 12824371 intron variant A/G snv 0.59 2
rs28721484
PXYLP1 ; ZBTB38
3 141334437 intron variant C/T snv 0.22 2
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 3
rs765876
HIVEP2
6 142864754 intron variant A/G snv 0.43 1
rs6587515 1 150636412 regulatory region variant G/A snv 7.2E-02 2
rs6440919 3 153982187 upstream gene variant C/T snv 0.47 1
rs1650505 5 158602726 intergenic variant G/A snv 0.22 2
rs9313296 5 165950694 intergenic variant G/C snv 0.13 1
rs551544003
SH3RF1
4 169152874 intron variant G/A snv 2.9E-04 1
rs630372 1 177916627 intron variant G/A;T snv 1
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs12517906 5 180743819 upstream gene variant C/A;T snv 0.11 1
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs6793368
LOC105374257 ; DGKG
3 186122654 intron variant C/T snv 0.82 1
rs397778224 16 19912366 regulatory region variant -/C delins 0.21 2
rs9940317
LOC105371117
16 19977530 intergenic variant A/G snv 0.21 1