Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs11983997 0.925 0.120 7 73524914 upstream gene variant G/A;C snv 5
rs6760250
ZNF512
0.925 0.120 2 27589385 intron variant G/A;C snv 5
rs7777102 7 73643687 intergenic variant A/G;T snv 5
rs17309872
ACSS2 ; GSS
0.925 0.080 20 34927985 downstream gene variant A/C;G;T snv 4
rs6727388
LINC01460
0.925 0.120 2 27709720 intron variant A/G;T snv 4
rs10485505
ITCH
1.000 0.080 20 34437762 intron variant C/G;T snv 3
rs6087664
TRPC4AP
1.000 0.080 20 35038413 intron variant C/A;G;T snv 3
rs6120816
TRPC4AP
1.000 0.080 20 35056555 intron variant G/A;C snv 3
rs1018503
NCOA6
20 34737712 intron variant T/A;G snv 2
rs11700080
ITCH
20 34458956 intron variant A/C;G snv 2
rs11906318
MMP24-AS1-EDEM2 ; EDEM2
20 35141639 intron variant A/C;T snv 2
rs12465955 2 127249498 non coding transcript exon variant A/G;T snv 2
rs12477670
MYO7B
2 127576951 intron variant A/C;G snv 2
rs12622436
MAP3K2
2 127324106 intron variant C/A;T snv 2
rs12625272
ASIP
20 34206355 intron variant C/A;G;T snv 2
rs13038810 20 36282301 intergenic variant A/C;G snv 2
rs13407823
MYO7B
2 127581139 intron variant A/G;T snv 2
rs17092215
TRPC4AP
20 35008110 intron variant C/G;T snv 2
rs17092750
C20orf173
20 35527132 3 prime UTR variant A/G;T snv 2
rs17310467
MYH7B ; GSS
20 34957813 intron variant A/G;T snv 2
rs17336615
NFS1
20 35674089 non coding transcript exon variant A/C;G snv 2
rs17406518
MMP24OS ; MMP24-AS1-EDEM2 ; PROCR
20 35211373 intron variant A/C;G snv 2