Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9377188
LOC105378047 ; UST
6 149030245 intron variant C/G;T snv 1
rs9376307 6 137962128 intron variant C/T snv 0.28 1
rs9375701
L3MBTL3
0.827 0.160 6 130062912 intron variant C/T snv 0.53 6
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs9350
EXO1
0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs9323205 14 51119749 regulatory region variant A/G snv 0.21 1
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs9261204
ZNRD1ASP
0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs9257445 6 28981429 upstream gene variant G/C snv 0.34 2
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs917570055
GZMM
0.882 0.360 19 547342 start lost A/G snv 7
rs917411291
GZMM
0.851 0.360 19 544072 start lost A/C;G snv 9
rs915894
NOTCH4
1.000 0.080 6 32222613 missense variant T/G snv 0.35 0.36 3
rs9138
SPP1
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs912593
LINC00457 ; LINC02343
13 34458354 intron variant G/A snv 0.22 1
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs905883
ERBB4
0.851 0.120 2 212323745 intron variant C/G;T snv 6
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs895919 11 132360808 regulatory region variant T/C snv 0.38 2
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs8898
CTSB
0.925 0.120 8 11845033 3 prime UTR variant T/C snv 0.37 5