Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 3
rs11924032
SLC2A2
3 171017310 intron variant G/A snv 0.29 3
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 4
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs3765467
GLP1R
1.000 0.080 6 39065819 missense variant G/A;C;T snv 3.6E-02 1.2E-02 3
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 3
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5