Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6691768
NFIA
1.000 0.080 1 61326191 intron variant G/A;C snv 1
rs531930
NKAIN2
1.000 0.080 6 124422361 intron variant A/G;T snv 1
rs45565037
PHLDB1
1.000 0.080 11 118625403 intron variant G/A snv 0.20 1
rs11875687
PTPN2
1.000 0.080 18 12843138 intron variant T/C snv 0.17 1
rs72975916
PTPRK
1.000 0.080 6 127972910 intron variant C/T snv 0.12 1
rs9491896
PTPRK
1.000 0.080 6 127979804 intron variant G/A snv 8.5E-02 1
rs13401064
STAT4
1.000 0.080 2 191105604 intron variant C/G snv 8.5E-02 1
rs6715106
STAT4
1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02 1
rs6752770
STAT4
1.000 0.080 2 191108837 intron variant A/G snv 0.31 1
rs10484718
THEMIS
1.000 0.080 6 127859906 intron variant A/T snv 8.6E-02 1
rs4897233
THEMIS
1.000 0.080 6 127835743 intron variant A/G snv 0.38 1
rs6441961
UQCRC2P1
1.000 0.080 3 46310893 non coding transcript exon variant T/C snv 0.74 1
rs11851414
ZFP36L1
1.000 0.080 14 68792785 intron variant T/C snv 0.25 1
rs1250557
ZMIZ1
1.000 0.080 10 79306017 intron variant G/T snv 0.63 1
rs6032606
ZNF335
1.000 0.080 20 45967568 missense variant C/A;G snv 0.84 1
rs11217040 0.925 0.200 11 118809939 regulatory region variant C/A snv 0.19 2
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 2
rs12068671 0.925 0.160 1 172711891 intergenic variant T/C snv 0.23 2
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 2
rs17264332 0.925 0.200 6 137684378 intron variant A/G;T snv 2
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 2
rs62323881 0.925 0.200 4 122117140 regulatory region variant C/A;T snv 2
rs6696533 0.925 0.200 1 198764438 intergenic variant T/C snv 0.28 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2