Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7116456 11 23933767 intergenic variant T/C snv 0.97 2
rs1451538
SLC28A1
15 84921399 intron variant T/C snv 0.95 2
rs996004 4 45076991 intergenic variant G/A snv 0.95 1
rs210131
GGNBP1
1.000 0.080 6 33567689 intron variant T/C snv 0.95 2
rs648425
PTGFR
1 78421523 intron variant T/C snv 0.95 2
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs6461992
HOXA10-HOXA9 ; HOXA11 ; HOXA10
1.000 0.120 7 27181212 3 prime UTR variant A/G snv 0.93 5
rs4722675
HOTTIP
7 27204343 intron variant A/G snv 0.93 4
rs3735533
HOTTIP
7 27206274 non coding transcript exon variant T/C snv 0.93 4
rs4775769
LOC105370809 ; FBN1
15 48647691 intron variant T/G snv 0.93 2
rs6565174
LOC101928595
16 30100583 intron variant A/C snv 0.93 2
rs10883543
PAX2
10 100792995 intron variant G/T snv 0.91 1
rs4551692
PAX2
10 100796696 intron variant G/A snv 0.91 2
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs2059752
LOC101927896
2 234885108 intron variant C/T snv 0.90 1
rs555625
PRDM6
5 123117450 intron variant C/T snv 0.90 1
rs2023843
HOTTIP
7 27203602 intron variant C/T snv 0.90 2
rs8002127 13 73250287 intergenic variant C/T snv 0.90 1
rs7034315
PALM2AKAP2
9 109593612 intron variant A/G snv 0.90 1
rs4842313 12 79502039 intron variant C/T snv 0.89 1
rs11158609
NEDD8 ; NEDD8-MDP1
14 24219608 intron variant G/A snv 0.89 2
rs2504776
WASF2
1 27443969 intron variant T/C snv 0.88 1
rs7406910
HOXB7
17 48610894 missense variant T/C snv 0.88 0.88 3
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6