Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 8