Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3850370
NRXN3
1.000 0.080 14 78068563 intergenic variant G/T snv 0.68 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs1049434
SLC16A1
0.925 0.120 1 112913924 missense variant A/T snv 0.59 0.66 2
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 32
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs4636297
EGFL7 ; MIR126
0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 8
rs7248320
CARD8 ; CARD8-AS1
0.776 0.160 19 48256972 non coding transcript exon variant G/A snv 0.65 8
rs1732786
DTX1
1.000 0.080 12 113057841 5 prime UTR variant G/A snv 0.65 1
rs7671905
CFI
1.000 0.080 4 109801730 intron variant T/C snv 0.64 1
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs2227928
ATR
0.851 0.200 3 142562770 missense variant A/G snv 0.55 0.63 5
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 15
rs1414493 1.000 0.080 1 241523216 upstream gene variant A/G snv 0.62 1
rs6062251
MIR133A2 ; MIR1-1HG
1.000 0.080 20 62565060 non coding transcript exon variant T/C snv 0.58 0.62 1
rs861537
XRCC3 ; KLC1 ; LOC112268131
1.000 0.080 14 103700738 intron variant C/T snv 0.61 0.61 1
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs9390123
PHACTR2
1.000 0.080 6 143622177 intron variant T/C snv 0.60 1
rs2301113
HIF1A-AS3 ; HIF1A
0.925 0.120 14 61739830 intron variant C/A snv 0.60 2
rs11778573
CCN4
0.851 0.080 8 133216687 intron variant T/G snv 0.59 4
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs1126497
EPCAM
0.716 0.200 2 47373967 missense variant T/C snv 0.51 0.58 14
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 6