Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3836790
SLC6A3
0.882 0.080 5 1411740 intron variant -/ACATACACACTCAGACACACATACCATGCA ins 5
rs28363170
SLC6A3
0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs316019
SLC22A2
0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs121912594
CPS1
0.882 0.160 2 210675762 missense variant A/C snv 6
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs201739205
LOC108783654 ; HSD17B1
0.851 0.200 17 42552898 5 prime UTR variant A/C snv 7.8E-03 8.2E-03 5
rs35036378
ESR2
0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5
rs3761581
APLN
0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs7201
MMP2
0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37 4
rs1372503923
ITGA2
0.925 0.160 5 53048731 missense variant A/C snv 3
rs1050606
ANXA5
1.000 0.080 4 121696891 5 prime UTR variant A/C snv 0.50 2
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 2
rs2146204
LINC00970
1 168904861 intron variant A/C snv 0.13 1
rs403814
L3MBTL4
18 6282594 intron variant A/C snv 0.27 1
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 1
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 1
rs4900318
BDKRB2
14 96222623 intron variant A/C snv 0.54 1
rs751019
PTK2B
8 27451068 missense variant A/C snv 0.44 0.41 1
rs7961152
LOC105369699 ; BCAT1
12 24828677 intron variant A/C snv 0.61 1