Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10428766 6 150052058 intergenic variant C/T snv 0.19 1
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs10471939 5 55180855 intergenic variant T/A snv 0.11 1
rs10473333 5 43866494 intergenic variant T/A snv 6.4E-02 1
rs10481172
CCDC26
8 128993202 intron variant A/G snv 0.69 1
rs10508366 10 8735729 intergenic variant C/T snv 0.20 1
rs10542411 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 2
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs1059091
IFITM2
11 309127 missense variant A/C;G;T snv 0.42 1
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs1061407
GLDC
9 6532544 3 prime UTR variant G/A snv 0.68 1
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs1071849
UBXN11 ; CD52
1 26320235 missense variant A/G snv 0.67 0.70 1
rs10767658
BDNF-AS
11 27650705 intron variant C/G;T snv 2
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 6
rs10777163
POC1B
12 89436943 intron variant T/C snv 0.23 1
rs10794666
LOC107984932 ; RUNX3
1 24924339 intron variant C/T snv 0.45 1
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs10822220 10 63841301 intron variant A/G snv 0.17 1
rs10852622
ZFPM1
16 88490472 intron variant A/G snv 0.35 2
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs10864462
PEX14
1 10552101 intron variant A/T snv 0.11 1
rs10882899
FRAT2 ; LOC105378448
10 97336188 intron variant G/C snv 0.49 1
rs10893844 11 128315955 regulatory region variant G/C snv 0.36 2