Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7993418
FLT1
0.925 0.120 13 28308924 synonymous variant G/A snv 0.80 0.67 2
rs371609024
FUT8
0.925 0.120 14 65629530 missense variant A/G snv 4.0E-06 2
rs199474357
HLA-A
0.925 0.120 6 29942790 missense variant T/C;G snv 2
rs4795218
HNF1B ; LOC105371754
0.925 0.120 17 37718512 intron variant A/G snv 0.82 2
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 2
rs200349340
HOTAIR
0.925 0.120 12 53962704 non coding transcript exon variant T/A;G snv 2
rs201753355
HTATSF1P2 ; NQO2
0.925 0.120 6 3019647 missense variant G/A;C snv 2.0E-05 2
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs1318
LOC101928045 ; PITPNC1
0.925 0.120 17 67695266 3 prime UTR variant A/G snv 0.30 2
rs782095550
MANF
0.925 0.120 3 51386267 missense variant T/C snv 2
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs141095230
MGMT
0.925 0.120 10 129536277 missense variant C/A;T snv 8.0E-06; 5.2E-05 2
rs587778992
MLH1
0.882 0.200 3 37050606 stop gained C/T snv 2
rs63751412
MSH2
0.882 0.200 2 47429869 stop gained C/A;G;T snv 8.0E-06; 4.0E-06 2
rs3021088
ND2 ; COX1
0.925 0.120 MT 5460 missense variant G/A snv 2
rs767964519
NFE2L2
0.925 0.120 2 177231869 missense variant T/C snv 4.0E-06 2
rs1034925236
NR5A2
0.925 0.120 1 200048258 missense variant G/C snv 2
rs138147246
OGG1
0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs139632793
OGG1
0.925 0.120 3 9751114 missense variant G/C snv 5.2E-05 1.7E-04 2
rs145574072
OGG1
0.925 0.120 3 9754765 synonymous variant T/C snv 4.0E-06 2
rs149243735
OGG1
0.925 0.120 3 9751076 missense variant C/A snv 4.0E-06 2
rs5757573
PDGFB
0.925 0.120 22 39237617 intron variant C/T snv 0.57 2
rs1235228469
PIK3CB
0.925 0.120 3 138684714 missense variant C/A snv 8.0E-06 2
rs1412335442
PIK3CG
0.925 0.120 7 106868317 missense variant G/T snv 7.0E-06 2
rs1448106115
PMS2
0.925 0.120 7 5989944 missense variant T/C snv 4.0E-06 2