Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2143416 1.000 0.080 1 186684633 upstream gene variant A/C;T snv 0.27 1
rs62355902 1.000 0.080 5 56757896 intergenic variant A/T snv 0.15 1
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 1
rs587782652
ATM ; C11orf65
0.851 0.320 11 108335105 missense variant T/C snv 3.2E-05 4.2E-05 1
rs1236971182
CDKN1A
1.000 0.080 6 36684381 missense variant C/T snv 8.1E-06 1
rs757172284
GNAO1
1.000 0.080 16 56340838 missense variant G/A snv 1.6E-05 1
rs6596100
HSPA4
0.925 0.080 5 133071366 intron variant C/T snv 0.24 1
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 1
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 1
rs11977670
LOC107986854
1.000 0.080 7 140242504 downstream gene variant G/A snv 0.39 1
rs1230666
MAGI3
0.925 0.200 1 113630788 intron variant A/G snv 0.90 1
rs6788895
SIAH2
0.882 0.080 3 150750021 intron variant G/T snv 0.18 1
rs747097215
SLC12A9
1.000 0.080 7 100856990 missense variant C/T snv 2.0E-05 2.1E-05 1
rs6453204
SV2C
1.000 0.080 5 76143375 intron variant A/G snv 0.90 1
rs11196175
TCF7L2
0.925 0.160 10 112976855 intron variant T/C snv 0.20 1
rs10043985 0.925 0.080 5 111065770 upstream gene variant A/C snv 5.2E-02 2
rs1034794 0.925 0.080 7 124801348 intergenic variant A/T snv 0.69 2
rs10515083 0.925 0.080 17 54886696 intergenic variant T/A snv 0.46 2
rs10759243 0.925 0.080 9 107543834 upstream gene variant C/A;T snv 2
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 2
rs10825036 0.882 0.080 10 53506471 intergenic variant T/G snv 0.21 2
rs10902845 0.925 0.080 10 122923791 intergenic variant T/C snv 3.0E-02 2
rs11045777 0.925 0.080 12 21126647 intron variant G/A snv 0.16 2
rs11055880 0.925 0.080 12 14257700 downstream gene variant C/G;T snv 2
rs11242675 0.925 0.080 6 1318643 downstream gene variant C/T snv 0.58 2