Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs2294021
CCDC22
0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs9469220 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 5
rs70993900 0.882 0.080 6 32618381 intergenic variant C/- delins 4.8E-02 3
rs2178077 1.000 0.080 12 130895928 intergenic variant G/A snv 8.8E-02 1
rs3888722 1.000 0.080 6 29771223 intergenic variant C/G snv 4.9E-02 1
rs861256
CD59
1.000 0.080 11 33725787 intron variant C/A;T snv 1
rs1865097
FCAR
1.000 0.080 19 54885805 intron variant G/A snv 0.32 1
rs1805672
KLRG1
1.000 0.080 12 9010581 3 prime UTR variant A/G snv 0.23 1
rs11084332
LAIR1
1.000 0.080 19 54369204 intron variant T/C snv 0.32 1
rs56802430
LAIR1
1.000 0.080 19 54366807 intron variant A/G snv 0.12 1
rs2287828
LAIR2
1.000 0.080 19 54502908 5 prime UTR variant G/A snv 9.0E-02 5.2E-02 1
rs35336528
LENG8
1.000 0.080 19 54456859 missense variant A/G snv 3.2E-02 2.8E-02 1