Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs3829109
CARD9 ; DNLZ
9 136362314 intron variant G/A snv 0.25 2
rs339416
DNAH5
5 13986417 regulatory region variant G/A snv 3.5E-02 1
rs225675
VTA1
6 142190999 intron variant A/G snv 0.40 1
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs10276674
DGKB
7 14882382 intron variant T/C;G snv 1
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 3
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs1974620 1.000 0.080 7 15025842 intergenic variant C/A;T snv 2
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 3
rs958444
SGCD
5 155978395 intron variant T/C snv 0.97 1
rs17066694 5 166334297 intergenic variant A/G snv 4.8E-02 1
rs2390732
CERS6
2 168749457 intron variant G/A snv 0.65 2
rs10497345
SPC25
2 168878291 intron variant G/C snv 0.11 1
rs477224
SPC25
2 168893973 intron variant C/T snv 0.62 1
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 5
rs34177044
SPC25
2 168897975 intron variant G/A snv 0.24 1
rs13387347
SPC25
2 168898336 intron variant T/C snv 0.49 1
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs492594
SPC25 ; G6PC2
1.000 0.080 2 168907666 missense variant G/C snv 0.50 0.43 2
rs2232326
SPC25 ; G6PC2
2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3
rs563694
ABCB11
2 168917561 intron variant C/A snv 0.75 2
rs16856247
ABCB11
2 168927903 intron variant C/T snv 6.6E-02 2
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 4