Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs6591182
EHBP1L1
0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs1201810520
EIF2AK3
0.925 0.160 2 88590497 missense variant C/T snv 2
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs1545224
FABP1
0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs1059122
FAM13A-AS1 ; FAM13A
0.882 0.160 4 88726273 3 prime UTR variant T/A snv 0.46 3
rs3017895
FAM13A-AS1 ; FAM13A
1.000 0.080 4 88728340 3 prime UTR variant A/G snv 0.19 1
rs1553553086
FARSB
0.827 0.280 2 222623699 missense variant C/T snv 9
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
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs26311
GHRLOS ; GHRL
1.000 0.080 3 10291242 5 prime UTR variant C/G snv 0.16 1
rs2629751
GLT8D2
0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs747432300
GPT ; LOC101928953
0.925 0.120 8 144504357 missense variant C/A;T snv 8.1E-06; 1.2E-04 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27