Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10051330
LINC02227
5 158392616 intron variant A/G;T snv 2
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10060615
SLC22A5
5 132373185 intron variant T/A;C snv 1
rs10062049 5 62258054 regulatory region variant C/T snv 0.16 2
rs10077885 5 115054424 regulatory region variant C/A snv 0.56 2
rs10078021 5 75742606 intergenic variant T/G snv 0.51 1
rs10087782
PTK2
8 140848521 intron variant T/C snv 0.43 1
rs10092965 8 8515975 intergenic variant A/G snv 0.43 2
rs10103353 8 81937217 intergenic variant C/T snv 0.35 1
rs1015291 12 19831845 intron variant A/G snv 0.55 1
rs1015538
ZKSCAN1
7 100028412 intron variant A/G snv 0.72 1
rs10164193
ASXL3
18 33581462 intron variant T/G snv 0.13 1
rs10166552
KCNE4
2 223171819 intron variant C/A;G;T snv 4.3E-03 2
rs10176996
LINC01808
2 19508931 intron variant C/T snv 0.69 1
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10184839 2 181081388 intron variant A/T snv 0.77 1
rs10193543
EXOC6B
2 72256200 intron variant T/G snv 0.13 1
rs10198275
ADCY3
2 24907673 intron variant A/C snv 0.53 1
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10228276
HOTTIP
7 27207660 downstream gene variant G/A snv 0.73 1
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs10260816
LOC102723446
7 45970501 intron variant C/A;G;T snv 2
rs10275663
GRB10
7 50729988 intron variant G/A snv 9.4E-02 2
rs1027989
LYN
8 55901862 intron variant G/A;C snv 3