Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1547014
CHEK2
1.000 0.040 22 28704723 intron variant T/C snv 0.64 1
rs790357
DLG2
1.000 0.040 11 83909897 intron variant C/G;T snv 1
rs4931170
FAR2
1.000 0.040 12 29235839 intron variant A/G snv 0.30 1
rs52809447
GGA3
1.000 0.040 17 75242427 missense variant T/C snv 7.3E-03 7.9E-03 1
rs7291444
PKDREJ
1.000 0.040 22 46260349 missense variant T/A;G snv 7.6E-03; 0.14 1
rs12093097
PTGFR
1.000 0.040 1 78489470 intron variant C/T snv 0.25 1
rs3753380
PTGFR
1.000 0.040 1 78490747 intron variant T/C snv 0.78 1
rs10306114
PTGS1
1.000 0.040 9 122370243 upstream gene variant A/G snv 8.0E-02 1
rs17588172 0.925 0.040 7 116513961 intergenic variant T/G snv 0.35 2
rs782006965
ADAMTS10
0.925 0.040 19 8589505 missense variant C/T snv 4.0E-06 2
rs766147142
FDXR
0.925 0.040 17 74863112 missense variant C/A;G;T snv 8.0E-06 2
rs770691402
FDXR
1.000 0.040 17 74866514 missense variant C/T snv 4.0E-06 2
rs12419342
RAPSN
1.000 0.040 11 47446993 intron variant C/T snv 0.61 2
rs4241366
SLCO2A1
0.925 0.040 3 134031326 intron variant G/A;C;T snv 2
rs1268656
SYNE2 ; ESR2
0.925 0.040 14 64180928 intron variant T/G snv 0.12 2
rs3211931
CD36
0.925 0.080 7 80668857 intron variant C/T snv 0.38 3
rs3766355
PTGFR
0.882 0.040 1 78491756 intron variant C/A;T snv 3
rs11568658
SNORD13G ; ABCC4
0.925 0.040 13 95210754 missense variant C/A snv 4.9E-02 3.0E-02 3
rs7081455 0.851 0.040 10 20349956 upstream gene variant G/A;T snv 4
rs747782 0.925 0.040 11 47919373 intergenic variant T/C snv 0.26 4
rs6445055
FNDC3B
0.925 0.040 3 172274597 intron variant G/A snv 0.24 4
rs7859156
LMX1B
0.851 0.040 9 126637749 intron variant T/C snv 0.74 4
rs74315341
MYOC ; MYOCOS
0.851 0.040 1 171636686 missense variant C/T snv 4
rs3793342
NOS3
0.851 0.040 7 150998107 intron variant G/A snv 0.13 4
rs743507
NOS3
0.882 0.200 7 151010400 intron variant C/T snv 0.77 4