Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs1553553086
FARSB
0.827 0.280 2 222623699 missense variant C/T snv 9
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs2234671
CXCR1
0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs10932029
ICOS ; LOC101927840
0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs1396171148
FARSB
0.851 0.200 2 222613892 missense variant T/G snv 5
rs1419129874
FARSB
0.851 0.200 2 222642894 missense variant A/G snv 7.0E-06 5
rs1466642025
FARSB
0.851 0.200 2 222631635 missense variant A/G snv 7.0E-06 5
rs1553554543
FARSB
0.851 0.200 2 222631606 missense variant T/C snv 5
rs843645
ACYP2
0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs3106796
COL3A1 ; LOC105373791
0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 3
rs3820998
TANK ; LOC105373719
0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs1201810520
EIF2AK3
0.925 0.160 2 88590497 missense variant C/T snv 2
rs1545224
FABP1
0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs26311
GHRLOS ; GHRL
1.000 0.080 3 10291242 5 prime UTR variant C/G snv 0.16 1
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs7664413
VEGFC ; LOC105377555
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25 7
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6