Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048369
GPC4
0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4
rs1062630
POU5F1
6 31170330 synonymous variant G/A snv 0.18 0.22 1
rs10885
PRRC2A
6 31636814 missense variant C/T snv 0.14 0.17 1
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs10947262
TSBP1-AS1 ; BTNL2
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 3
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1161098
LOC105369812 ; LINC02408
12 67453680 intron variant G/A snv 0.84 1
rs116671518
DKK2
4 107189709 intron variant T/C snv 1.9E-02 1
rs12154141 6 62460168 downstream gene variant A/C snv 0.20 1
rs12759054
SLC35F3
1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs138117677 16 3348899 TF binding site variant GGGACT/- delins 2.8E-02 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs200655768
TTN-AS1 ; TTN
2 178711222 synonymous variant G/A;T snv 1
rs200688486 6 32621223 regulatory region variant -/T delins 1
rs204992
PBX2
6 32189131 intron variant G/A snv 0.22 1
rs204994
PBX2
0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs204995
PBX2
1.000 0.120 6 32186508 non coding transcript exon variant A/G snv 0.21 0.27 2
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2153486 14 87737048 intron variant C/T snv 0.68 1
rs2213585
HLA-DRA
1.000 0.040 6 32445373 downstream gene variant G/A snv 0.61 2
rs2213586
HLA-DRA
1.000 0.040 6 32445317 downstream gene variant A/G snv 0.61 2
rs2227139 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 4
rs2239802
HLA-DRA
0.882 0.200 6 32444069 intron variant C/A;G;T snv 4
rs2239803
HLA-DRA
0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 4
rs2239804
HLA-DRA
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5