Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs1001703993
PPOX
0.882 0.120 1 161170696 missense variant G/A;T snv 8.0E-06 1.4E-05 3
rs10086568 1.000 0.120 8 7042814 upstream gene variant G/A snv 0.34 2
rs1047763
C1GALT1
0.925 0.120 7 7243938 3 prime UTR variant G/A snv 0.22 2
rs11264794
FCRL3
1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63 2
rs13124532
LOC645513 ; PDE5A
1.000 0.120 4 119495290 3 prime UTR variant C/T snv 0.10 2
rs1794275 1.000 0.120 6 32703471 downstream gene variant G/A snv 0.21 2
rs2364480
LTBR
0.925 0.120 12 6386109 synonymous variant C/A;T snv 0.77; 2.0E-05 2
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs373544789
FCAR
0.925 0.120 19 54889688 missense variant G/A;T snv 8.8E-05; 3.2E-05 2
rs3759334
LTBR
0.925 0.120 12 6382842 intron variant G/A snv 0.26 2
rs4227
SOX15 ; MPDU1
1.000 0.120 17 7587859 3 prime UTR variant G/T snv 0.71 0.67 2
rs7190997
ITGAX
1.000 0.120 16 31356857 intron variant T/C snv 0.52 2
rs9314614
GS1-24F4.2
1.000 0.120 8 6840209 intron variant C/G snv 0.61 2
rs1008898
C1GALT1
1.000 0.120 7 7233928 intron variant G/A;T snv 1
rs10488764
FDX1
1.000 0.120 11 110460907 intron variant G/A snv 0.18 1
rs1055901
SERPINB7
1.000 0.120 18 63805221 3 prime UTR variant T/C snv 0.61 1
rs1055902
SERPINB7
1.000 0.120 18 63805309 3 prime UTR variant C/T snv 0.59 1
rs11084377
FCAR
1.000 0.120 19 54875434 intron variant A/G;T snv 1
rs11150612 1.000 0.120 16 31346439 intergenic variant G/A snv 0.28 1
rs11264793
FCRL3
1.000 0.120 1 157677736 3 prime UTR variant A/T snv 0.28 1
rs12022418
LOC105371664
1.000 0.120 1 192565977 intron variant C/A snv 0.64 1
rs12716641 1.000 0.120 8 7041476 upstream gene variant T/A;C snv 1
rs1362970
NTN4 ; PGAM1P5
1.000 0.120 12 95658750 3 prime UTR variant C/A snv 0.47 1
rs1369270 1.000 0.120 2 153179546 intron variant T/C snv 1