Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7934276 11 100631600 regulatory region variant T/C snv 0.27 1
rs60583266
LINC01349
1 100635283 intron variant C/G snv 0.37 1
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs7141210 14 100716133 regulatory region variant T/C snv 0.55 2
rs12088882 1 100759064 intergenic variant C/T snv 0.45 1
rs2059846
ST8SIA4
5 100865206 intron variant T/A;C snv 1
rs36055153
NPAS2
2 100980158 intron variant G/A snv 0.12 1
rs733830
TBC1D8
2 101161857 intron variant T/C snv 0.68 1
rs28576226 15 101173463 downstream gene variant G/A snv 0.15 1
rs57105322
MSRA
8 10120812 intron variant G/A;T snv 1
rs12144133
UBE4B
1 10144128 intron variant T/G snv 0.37 1
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs6846071
BANK1
4 101481058 intron variant T/G snv 0.15 2
rs1037117 15 101528455 upstream gene variant G/A snv 0.28 1
rs6543087
MAP4K4
1.000 0.080 2 101699471 intron variant A/G;T snv 2
rs12787996
YAP1
11 102186337 non coding transcript exon variant C/A snv 0.31 1
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02 4
rs8113091 19 10239014 intergenic variant T/A;C snv 1
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs35879747
SUFU
10 102588937 intron variant T/A snv 0.18 1
rs10883756 10 102640355 upstream gene variant T/A;C snv 1
rs4807440
CNN2
19 1026478 upstream gene variant G/T snv 0.65 3
rs7917772
SFXN2
10 102727686 3 prime UTR variant G/A;C snv 0.46 3
rs2431320
PAM
5 102782681 intron variant C/T snv 0.31 1
rs972142 8 102824025 downstream gene variant A/G snv 0.38 1