Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs149104283
SLCO1B3-SLCO1B7
0.882 0.040 12 20930928 intron variant C/G;T snv 4
rs2228391
TAP2
0.882 0.160 6 32829996 missense variant T/C snv 1.3E-02 3.9E-03 3
rs116869525 0.925 0.160 6 32421366 intergenic variant C/T snv 3.5E-03 2
rs17193122 0.925 0.160 6 31367559 intron variant G/A;T snv 2
rs185386680 0.925 0.040 6 31207153 downstream gene variant A/G snv 1.2E-03 2
rs622871
CYP21A2 ; C2
1.000 0.040 6 31910718 intron variant A/C;G snv 2
rs9262631
HCG22
0.925 0.160 6 31056824 non coding transcript exon variant C/A;T snv 2
rs2596449
HCP5 ; HCG26
0.925 0.160 6 31470613 non coding transcript exon variant A/G snv 0.79 2
rs114291795
MICA
0.925 0.040 6 31409863 intron variant C/G snv 3.0E-02 2
rs7768644
MUC22
0.925 0.160 6 31034324 intron variant G/A snv 9.5E-02 2
rs56343172
PHLDB2
0.925 0.160 3 111868398 intron variant C/T snv 0.11 2
rs9263688
PSORS1C1
0.925 0.160 6 31124190 intron variant A/G snv 5.2E-02 2
rs17201248
SNHG32 ; SNORD48 ; SNORD52
0.925 0.160 6 31835353 non coding transcript exon variant C/G;T snv 4.3E-06; 2.8E-02 2
rs111618861 1.000 0.040 8 56131824 regulatory region variant AAA/-;A;AA;AAAA;AAAAA delins 5.9E-02 1
rs111703385 1.000 0.040 8 8642006 intergenic variant G/A;C snv 1
rs114431066 1.000 0.040 3 197381461 regulatory region variant C/T snv 1.3E-02 1
rs117767021 1.000 0.040 9 88685871 intergenic variant T/A snv 1.5E-02 1
rs148071215 1.000 0.040 14 82806309 intergenic variant G/A snv 2.0E-02 1
rs149020156 1.000 0.040 11 91940355 intergenic variant G/A snv 1.0E-02 1
rs16919354 1.000 0.040 8 53554028 intergenic variant T/G snv 3.3E-02 1
rs1811197 1.000 0.040 6 31359883 upstream gene variant G/A snv 0.15 1
rs202233001 1.000 0.040 20 21754716 upstream gene variant ACA/- del 3.2E-02 1
rs74997117 1.000 0.040 7 155060018 intergenic variant C/T snv 3.3E-02 1