Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10018951
TRAPPC11
1.000 0.080 4 183688220 intron variant C/T snv 0.18 1
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45 3
rs10032909
LINC01088
1.000 0.080 4 79049054 intron variant A/G snv 0.13 1
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs1003878
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs10048743
IKZF2
1.000 0.080 2 213025508 intron variant G/T snv 0.78 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1012507
TNFSF4 ; LOC100506023
1.000 0.080 1 173250332 intergenic variant G/T snv 0.32 1
rs10127175
IRAK1
1.000 0.080 X 154018721 missense variant A/T snv 5.1E-03 1.8E-02 1
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs10156091
ICA1
1.000 0.080 7 8147464 intron variant T/C snv 0.86 1
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10239340
TNPO3
1.000 0.080 7 129028456 intron variant T/A;G snv 1
rs10245867
JAZF1
0.925 0.080 7 28102567 intron variant G/T snv 0.37 2
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 3
rs10279821
TNPO3
1.000 0.080 7 129043493 intron variant T/A;C snv 1
rs1028488 1.000 0.080 6 170281387 upstream gene variant G/T snv 0.46 2
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs1039917
MFHAS1
1.000 0.080 8 8861340 intron variant G/A snv 0.31 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214