Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 6
rs771386507
HLA-B ; MIR6891
0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs1456079929
PGR
0.851 0.120 11 101042001 missense variant C/A snv 8.0E-06 5
rs540432391
CGB5
0.882 0.120 19 49043993 5 prime UTR variant G/A;C snv 5
rs7246045
CGB5
0.882 0.120 19 49042825 upstream gene variant T/G snv 2.9E-02 5
rs755378873
SLC13A5
0.851 0.120 17 6694197 missense variant C/A;T snv 4.0E-06 5
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs1444192401
KRT7
0.882 0.120 12 52235347 missense variant G/A snv 4
rs2287498
WRAP53 ; TP53
0.882 0.120 17 7689242 synonymous variant C/T snv 0.13 0.14 4
rs495139
ENOSF1
0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs67164370
RASSF2
0.851 0.120 20 4787830 intron variant -/AGGGACT ins 4
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs7313833 0.851 0.120 12 27930263 intergenic variant G/A snv 0.37 4
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 3
rs10098821
LINC00824
0.882 0.120 8 128546982 intron variant C/T snv 7.6E-02 3
rs1136905
HLA-DRB3 ; HLA-DRB5
0.882 0.120 6 32518660 missense variant T/A;C snv 4.2E-03 3
rs11683487
NMI
0.882 0.120 2 151286035 intron variant G/T snv 0.36 3
rs13063604
RUVBL1
0.882 0.120 3 128085887 intron variant G/A snv 0.23 3
rs147961867
MAPK3
0.882 0.120 16 30121998 missense variant T/C snv 5.6E-05 2.8E-05 3
rs1516982
LINC00824
0.882 0.120 8 128521400 intron variant A/G snv 0.16 3
rs1649942
NRG3
0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs1805129
CHEK2
0.882 0.120 22 28734470 synonymous variant T/C snv 3.6E-02 4.0E-02 3
rs186724
AHCYL1
0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs192876988
LOC105377300
0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 3
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 3