Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs3842570
CAPN10
0.925 0.160 2 240594824 intron variant -/CGGGAGGAGGGTGATGATTCTGTCCCAGGAGC delins 2
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs316019
SLC22A2
0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 5
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
rs7713645
PIK3R1
0.851 0.200 5 68231498 intron variant A/C snv 0.58 4
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs1372503923
ITGA2
0.925 0.160 5 53048731 missense variant A/C snv 3
rs2275703
CASQ1
0.925 0.080 1 160195305 intron variant A/C snv 0.38 3
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 3
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 2
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 2
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 2
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 2
rs151290
KCNQ1
1.000 0.080 11 2800385 intron variant A/C snv 0.67 2
rs1541276
MC5R
0.925 0.120 18 13825728 splice region variant A/C snv 0.17 0.19 2
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 2
rs16860234
IGF2BP2
0.925 0.080 3 185793096 intron variant A/C snv 0.33 2
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2