Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200312707 1.000 0.040 16 62031776 intron variant TA/- del 2
rs142484554 0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs200855945 0.925 0.040 12 26124961 5 prime UTR variant ACACGCACAC/-;ACACGCACACACACGCACAC delins 1.6E-02 3
rs201203751 0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs201569130 0.925 0.040 6 1402916 intergenic variant GACA/- delins 1.1E-02 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs34177316 0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs34807503 1.000 0.040 12 51525350 intergenic variant ATTTATTT/-;ATTT;ATTTATTTATTT delins 2
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs7225002 0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs8067056 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs9303521 0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs12938031 0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs199505 0.925 0.120 17 46782044 intron variant A/G snv 0.84 4
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs754593 1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3