Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs80356664
INS-IGF2 ; INS
0.882 0.120 11 2160878 missense variant C/G;T snv 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs786204848
DDX58
0.882 0.040 9 32488884 missense variant C/A snv 4
rs786204847
DDX58
1.000 9 32488039 missense variant T/G snv 2
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs774263008
FCRL3
1 157697767 missense variant C/T snv 4.0E-06 1
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs76857106
RNASEH2A ; HOOK2
1.000 0.120 19 12806782 missense variant G/A snv 3
rs7678445
KIAA1109
4 122361617 intron variant G/A;T snv 2
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 13
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs766061667
PIK3R2
19 18168775 missense variant C/T snv 4.1E-06 1
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs765797019
PIK3CD
1 9720754 missense variant C/T snv 3.3E-05 3.5E-05 1
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs761234173
CDH13
1.000 0.040 16 83783345 missense variant G/A snv 4.0E-06 2