Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 13
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs1314913
RAD51B
0.807 0.120 14 68232877 intron variant C/T snv 0.13 6
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 6
rs6974491
ELMO1
0.807 0.120 7 37334906 intron variant G/A snv 0.14 6
rs11856808
LINGO1
0.827 0.120 15 77680428 intron variant C/T snv 0.42 5
rs11871753
BRIP1
0.851 0.120 17 61779284 intron variant A/G snv 0.75 4
rs16945628
BRIP1
0.851 0.120 17 61789868 intron variant T/C snv 0.60 4
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
rs1816
KANSL1
0.882 0.200 17 46199252 intron variant A/G snv 0.14 3
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs2299941
PTEN
0.882 0.080 10 87944962 intron variant A/G snv 9.7E-02 3
rs740603
COMT
0.925 0.040 22 19957654 intron variant A/G snv 0.48 3
rs9472817
LOC101926934 ; SLC25A27
0.882 0.080 6 46673255 intron variant C/G;T snv 3
rs39399
RELN
0.925 0.040 7 103849545 intron variant G/A;T snv 2
rs4434401
CAST
0.925 0.040 5 96703321 intron variant T/C snv 0.45 2
rs3735273
DDC ; FIGNL1
1.000 7 50529166 intron variant C/T snv 0.25 0.27 1
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs623011 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 5