Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 4
rs8010717
LOC107984630
14 79944098 intron variant T/C snv 0.29 4
rs16890334 6 78846449 intergenic variant T/C snv 1.9E-03 3
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3
rs12899430
COX5A
15 74936759 intron variant T/C snv 0.37 2
rs13255193
FAM167A
8 11451683 intron variant T/C snv 0.47 2
rs1596724
LOC107986223
4 32554231 intergenic variant T/C snv 5.9E-02 2
rs10850411 12 114949991 intergenic variant T/C snv 0.34 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs7658266
ARSJ
4 113942550 intron variant T/A;C snv 2
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4