Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 4
rs4759313
HOTAIR
0.851 0.120 12 53965290 intron variant T/A snv 0.51 4
rs11644322
WWOX
0.925 0.120 16 79005703 intron variant C/T snv 0.22 3
rs2001389
SUFU
0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs3790844
NR5A2
0.882 0.200 1 200038304 intron variant A/C;G snv 3
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 2
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2
rs17458086
SLC2A13
0.925 0.120 12 40034837 intron variant T/C snv 1.1E-02 2
rs1810205
CUBN
0.925 0.120 10 16923228 intron variant A/G snv 0.47 2
rs2073389
SMARCB1
0.925 0.120 22 23791306 intron variant C/T snv 0.59 2
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 2
rs2457571
SLC22A3
0.925 0.120 6 160413796 intron variant T/C snv 0.62 2
rs2470353
XPC ; LOC107986063
0.925 0.120 3 14148768 intron variant G/A;C;T snv 0.41; 1.5E-04 2
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 2
rs2980874
TRIB1
0.925 0.120 8 125432546 intron variant G/A snv 0.30 2
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 2
rs3124761
SLC2A6
0.925 0.120 9 133474633 intron variant T/C snv 0.80 2
rs34852782
PRKAG2
0.925 0.120 7 151869086 intron variant -/A;AG ins 2
rs3729587
XPC
0.925 0.120 3 14167125 intron variant G/C snv 0.31 0.34 2
rs3731055
XPC ; LSM3
0.925 0.120 3 14178939 intron variant C/T snv 1.9E-02 2