Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2737713
LGALS8 ; LOC107985367
1.000 0.120 1 236537507 missense variant T/A snv 2
rs111945767 1.000 0.120 6 32549268 downstream gene variant G/C snv 0.45 1
rs11466316
TGFB1
1.000 0.120 19 41353431 5 prime UTR variant G/A;T snv 1
rs12653117
SEMA5A
1.000 0.120 5 9386473 intron variant C/T snv 0.14 1
rs150881176
HLA-A
1.000 0.120 6 29979963 downstream gene variant T/C snv 1
rs16862847
CHRNA1
1.000 0.120 2 174764872 intron variant T/C snv 0.14 1
rs17209237
NR3C1
1.000 0.120 5 143277647 downstream gene variant A/G snv 0.18 1
rs231770 1.000 0.120 2 203864430 upstream gene variant C/T snv 0.42 1
rs3753381
SLAMF1
1.000 0.120 1 160629620 intron variant G/A snv 0.31 1
rs3761389
AIRE
1.000 0.120 21 44285055 upstream gene variant G/A snv 0.14 1
rs3792785
TNIP1
1.000 0.120 5 151072089 intron variant T/C snv 0.13 1
rs4263037
TNFRSF11A
1.000 0.120 18 62349000 intron variant G/A snv 0.61 1
rs4361859 1.000 0.120 9 97062415 regulatory region variant G/A snv 0.77 1
rs564353179
TTN ; LOC101927055
1.000 0.120 2 178780121 missense variant C/G snv 9.6E-05 9.1E-05 1
rs6998967
LOC105375922
1.000 0.120 8 80451970 intron variant G/A snv 0.23 1
rs8058694
ABCC6
1.000 0.120 16 16185006 missense variant G/T snv 0.42 0.43 1
rs8058696
ABCC6
1.000 0.120 16 16185012 synonymous variant G/C;T snv 0.42 1
rs9963862
RBBP8
1.000 0.120 18 23007948 intron variant G/A;C snv 1
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs1634718
MUC22
0.925 0.160 6 31005088 regulatory region variant A/G snv 0.20 3
rs9270986
HLA-DRB1
0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 3
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs2071591
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.925 0.160 6 31548022 intron variant G/A;C snv 2