Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2107301
VDR
0.807 0.120 12 47861787 intron variant G/A snv 0.26 7
rs11574143
VDR
0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 5
rs2238135
VDR
0.882 0.160 12 47884407 intron variant C/G snv 0.26 4
rs11168314
VDR
0.925 0.080 12 47936846 intron variant G/A snv 0.23 2
rs2239182
VDR
0.925 0.080 12 47861628 intron variant T/C snv 0.51 2
rs2408876
VDR
0.925 0.080 12 47879782 intron variant T/A;C snv 2
rs7299460
VDR
0.925 0.080 12 47902485 intron variant C/T snv 0.43 2
rs1529916
USP7
0.851 0.120 16 8897333 intron variant G/A snv 0.26 4
rs72551387
UGT2B17
0.882 0.080 4 68568232 missense variant C/A snv 5.7E-03 5.7E-03 3
rs1902023
UGT2B15
0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 4
rs4148269
UGT2B15
0.882 0.080 4 68647129 missense variant T/G snv 0.55 0.49 3
rs13112099
UGT2B15
0.925 0.080 4 68672015 upstream gene variant T/G snv 0.53 2
rs3100
UGT2B15
0.925 0.080 4 68646936 3 prime UTR variant G/A snv 0.50 2
rs7686914
UGT2B15
0.925 0.080 4 68672197 upstream gene variant T/A;C snv 2
rs7696472
UGT2B15
0.925 0.080 4 68672462 upstream gene variant G/A snv 0.53 2
rs11913319
TXNRD2
0.925 0.080 22 19880016 intron variant C/G snv 0.26 2
rs4485648
TXNRD2
0.925 0.080 22 19931882 intron variant T/A;C snv 2
rs2301241
TXN
0.827 0.160 9 110257228 upstream gene variant G/A;T snv 4