Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs1689040 12 89584456 intron variant C/G;T snv 4
rs1830084
SRPRB ; LOC105374116 ; TF
0.882 0.160 3 133789620 3 prime UTR variant A/G;T snv 4
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs2586886
KCNK3
1.000 0.080 2 26709163 intron variant C/G;T snv 4
rs34071855
CASZ1
1 10738432 intron variant C/G;T snv 4
rs3794695
HPR ; TXNL4B
16 72063928 intron variant C/A;T snv 4
rs41274050
ASAH2B ; A1CF
10 50814012 missense variant C/A;T snv 4.0E-06; 5.3E-03 4
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs4820323
MAFF ; PLA2G6
22 38203760 non coding transcript exon variant C/A;G;T snv 4
rs60695258
AFF1
4 87101557 intron variant C/A;T snv 4
rs640065
NEK10
3 27322446 intron variant T/A;C snv 4
rs72831345
CABCOCO1
10 61758990 intron variant G/A;C snv 4
rs8071884
PGS1
17 78401977 intron variant C/A;G;T snv 4
rs10826334 10 59620724 intron variant C/A;G snv 3
rs11072518 15 74942269 upstream gene variant T/A;C snv 3
rs112640876
LSP1
11 1873813 intron variant A/G;T snv 3
rs13280442 8 11610048 intergenic variant C/A;G snv 3
rs1716983
ULK4
1.000 0.160 3 41922636 intron variant G/A;C;T snv 3
rs2328223 20 17865277 intergenic variant A/C;G;T snv 3