Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003878
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs1003879
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32331815 intron variant G/A snv 0.41 1
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs1005133 1.000 0.120 22 19750832 intergenic variant C/T snv 0.20 1
rs1005753
PADI2
1.000 0.120 1 17118274 intron variant G/T snv 0.55 1
rs10088748
SGCZ
1.000 0.120 8 14611016 intron variant C/A snv 0.51 1
rs10097964 1.000 0.120 8 21125392 intron variant G/A snv 2.6E-02 1
rs10106
FPGS
0.851 0.200 9 127813796 3 prime UTR variant T/C snv 0.45 4
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10174098
ITGAV
0.882 0.200 2 186628015 intron variant G/A snv 0.62 3
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs10175798 1.000 0.120 2 30226728 upstream gene variant G/A snv 0.51 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs1018430
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32313911 intron variant C/T snv 0.25 1
rs1018431
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32313899 intron variant G/A snv 0.25 1
rs1018433
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32313733 intron variant A/T snv 0.21 1
rs1018434
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32313583 intron variant T/C snv 0.21 1
rs10203477
LINC01185
0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs10209110
AFF3
1.000 0.120 2 100056230 intron variant C/T snv 0.47 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10263447
NPSR1 ; NPSR1-AS1
1.000 0.120 7 34820377 intron variant G/C snv 0.14 1
rs10275421
LNCPRESS1
1.000 0.120 7 101299780 non coding transcript exon variant G/A snv 7.2E-02 1
rs1033500
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32339605 missense variant G/A snv 0.40 0.33 2
rs1034323 1.000 0.120 6 30400858 intergenic variant C/T snv 0.43 1