Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6517774 21 17449955 non coding transcript exon variant A/G snv 0.34 1
rs1889740
ARNT
1 150827279 intron variant C/T snv 0.42 1
rs11571319
CTLA4
2 203874215 downstream gene variant G/A snv 0.17 1
rs774263008
FCRL3
1 157697767 missense variant C/T snv 4.0E-06 1
rs1052237
NUS1
6 117694118 stop gained T/C;G snv 8.8E-05 8.4E-05 1
rs1331108652
PIK3CB
3 138694820 stop gained G/A snv 4.0E-06 1
rs765797019
PIK3CD
1 9720754 missense variant C/T snv 3.3E-05 3.5E-05 1
rs766061667
PIK3R2
19 18168775 missense variant C/T snv 4.1E-06 1
rs1333739
RAVER2
1 64827766 intron variant A/G;T snv 0.62 1
rs2780889
RAVER2 ; JAK1
1 64833108 3 prime UTR variant A/T snv 0.52 1
rs8176928
TRAP1 ; DNASE1
16 3656184 missense variant A/G snv 1.0E-03 4.0E-03 1
rs8734
TTTY14
Y 18992540 non coding transcript exon variant G/A snv 1
rs55882956
TYK2
19 10359243 missense variant G/A;C snv 7.2E-03; 4.1E-06 1
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs10932019 2 203764087 downstream gene variant G/A;C snv 2
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 2
rs12115114 1.000 0.080 8 63477322 non coding transcript exon variant A/G;T snv 2
rs12992492 1.000 0.040 2 203836831 intergenic variant A/G snv 0.40 2
rs1355208 2 30222456 intergenic variant A/G snv 0.65 2
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 2
rs2108225 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 2
rs2155433 11 118742212 intron variant G/A snv 0.24 2
rs4626515 7 140204330 intergenic variant T/C snv 0.22 2
rs636393 6 137686393 intron variant G/T snv 0.66 2
rs975730 8 128303768 intergenic variant G/A snv 0.45 2