Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944888 0.925 0.080 15 90817292 upstream gene variant C/G snv 7.7E-02 2
rs17147338 0.925 0.080 4 69460168 intergenic variant C/A;T snv 2
rs171866 0.925 0.080 6 115870638 intergenic variant G/A snv 0.73 2
rs17302090 0.925 0.080 X 67535561 downstream gene variant G/A snv 8.5E-02 2
rs1963562 0.925 0.080 12 38269094 intergenic variant C/T snv 0.30 2
rs197057 0.925 0.080 16 1082015 upstream gene variant C/G snv 0.53 2
rs1994198 0.925 0.080 15 46360969 upstream gene variant C/T snv 0.47 2
rs2387084 0.925 0.080 16 74054192 non coding transcript exon variant T/G snv 0.28 2
rs2611489 0.925 0.080 10 46070933 regulatory region variant C/G;T snv 2
rs268091 0.925 0.080 5 39506521 regulatory region variant G/C snv 0.36 2
rs2836626 0.925 0.080 21 38686514 intergenic variant G/T snv 0.19 2
rs4631830 0.925 0.080 10 46052478 upstream gene variant A/G snv 0.43 2
rs4775302 0.925 0.080 15 46347610 intron variant G/A snv 0.49 2
rs4955720 0.925 0.080 3 170310812 downstream gene variant A/C;T snv 2
rs497844 0.925 0.080 5 112849794 intron variant A/G snv 0.64 2
rs585224 0.925 0.080 12 52529088 regulatory region variant A/G snv 0.66 0.50 2
rs5945572 0.882 0.160 X 51486831 downstream gene variant A/G snv 2
rs7127900 0.882 0.160 11 2212344 intergenic variant A/C;G snv 2
rs7837688 0.925 0.080 8 127527115 intergenic variant T/G snv 0.91 2
rs7920517 0.925 0.080 10 46063201 upstream gene variant C/G;T snv 2
rs817826 0.925 0.080 9 107394019 intergenic variant C/T snv 0.81 2
rs902774 0.925 0.080 12 52880120 regulatory region variant G/A snv 0.12 2
rs35605
ABCC1
0.925 0.080 16 16068162 synonymous variant T/C snv 0.79 0.84 2
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 2
rs17309872
ACSS2 ; GSS
0.925 0.080 20 34927985 downstream gene variant A/C;G;T snv 2