Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10934524 3 96431316 intergenic variant C/G;T snv 1
rs12143832 1 21378943 regulatory region variant T/C snv 0.44 1
rs138762279 5 174283195 intergenic variant T/- del 0.34 1
rs1416280 6 102438768 intergenic variant C/G snv 0.35 1
rs1425609 3 162964207 intergenic variant G/A snv 0.37 1
rs145672791 21 13377702 intergenic variant G/A snv 8.1E-03 1
rs1487614 4 42267463 non coding transcript exon variant T/C snv 0.65 1
rs2031577 10 4007811 intergenic variant A/G snv 0.53 1
rs2882281 13 89970201 intergenic variant C/A;G;T snv 1
rs3106598 13 61104778 intron variant G/A snv 0.43 1
rs6813479 4 136739228 intergenic variant T/A;C snv 1
rs6915183 6 166292681 intergenic variant A/G;T snv 1
rs7315621 12 131600651 upstream gene variant G/A snv 0.41 1
rs7493138 14 28552722 intergenic variant C/T snv 0.38 1
rs9592783 13 71309082 intergenic variant G/A snv 0.24 1
rs9616906 22 50666252 upstream gene variant G/A;C snv 1
rs9664222 10 87578876 intergenic variant A/C snv 0.84 1
rs4148546
ABCC4
13 95028031 intron variant G/A snv 0.55 1
rs3847687
ADGRD1
12 131040508 intron variant C/A;T snv 0.35 1
rs4732038
AKR1B15
7 134565570 intron variant A/C snv 0.51 0.52 1
rs2440012
ANKRD20A9P
13 18865983 intron variant C/A;G snv 1
rs10256972
C7orf50
7 999367 intron variant A/C snv 0.62 1
rs9841144
CADM2
3 85482049 intron variant A/T snv 0.17 1
rs9876781
CCDC51 ; ATRIP ; ATRIP-TREX1
3 48445934 intron variant A/G;T snv 1
rs2024714
CDH4
20 61637438 intron variant C/T snv 0.60 1