Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11079786 1.000 0.040 17 47728550 upstream gene variant G/A snv 0.27 1
rs11258303 1.000 0.040 10 6363572 regulatory region variant C/A;T snv 1
rs112799045 1.000 0.040 7 2899718 intergenic variant G/A;C;T snv 1
rs12191243 1.000 0.040 6 135125688 intergenic variant C/G snv 0.20 1
rs12271161 1.000 0.040 11 117109195 downstream gene variant G/A;T snv 1
rs1951459 1.000 0.040 6 166989048 intron variant G/A snv 0.42 1
rs1985378 1.000 0.040 22 39282307 downstream gene variant A/G snv 0.48 1
rs201295667 1.000 0.040 20 22649878 intergenic variant C/- del 8.5E-04 1
rs2517532 0.925 0.120 6 31050630 upstream gene variant A/G snv 0.60 1
rs34477738 1.000 0.040 9 5447227 upstream gene variant A/G snv 0.12 1
rs34509786 1.000 0.040 3 12264417 intergenic variant T/G snv 0.17 1
rs35703946 1.000 0.040 16 85987899 intron variant G/A snv 0.12 1
rs4820437 1.000 0.040 22 41365286 upstream gene variant T/C snv 0.42 1
rs57145876 1.000 0.040 1 113275045 intergenic variant A/T snv 3.1E-02 1
rs57938373 1.000 0.040 3 39294547 intron variant C/T snv 0.15 1
rs59183580 1.000 0.040 11 95692306 intron variant A/G snv 0.12 1
rs6505765 1.000 0.040 18 12782850 downstream gene variant C/A;G snv 1
rs6603785 1.000 0.040 1 1251122 non coding transcript exon variant A/T snv 0.21 1
rs66749983 1.000 0.040 13 42489695 downstream gene variant A/T snv 0.29 1
rs7090530 0.851 0.160 10 6068912 downstream gene variant C/A snv 0.59 1
rs736374 0.925 0.080 11 35245397 regulatory region variant G/A snv 0.29 1
rs7583027 1.000 0.040 2 62317256 intergenic variant A/C snv 0.74 1
rs9293291 1.000 0.040 5 72399010 regulatory region variant G/A;T snv 1
rs11783023 1.000 0.040 8 140629163 intron variant C/T snv 0.70 1
rs2473808 1.000 0.040 1 19312389 5 prime UTR variant T/C snv 0.69 1