Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1451506414
SLC22A12
0.882 0.200 11 64598561 synonymous variant G/A snv 4
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2276415
AQP11 ; CLNS1A
0.882 0.160 11 77590296 missense variant G/A snv 0.14 0.13 6
rs2093266
SERPINA5 ; SERPINA4
1.000 0.080 14 94566450 intron variant G/A snv 0.15 1
rs1955656
SERPINA5
1.000 0.080 14 94579038 intron variant G/A snv 0.14 1
rs753482595
SLC2A9
0.925 0.200 4 9920389 missense variant T/C snv 8.0E-06 1.4E-05 3
rs561633150
SLC2A9
0.925 0.200 4 9980627 missense variant C/T snv 6.1E-04 9.1E-05 2