Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869736
CORO1B ; PTPRCAP
0.925 0.080 11 67437991 3 prime UTR variant C/A snv 0.53 3
rs868903
MUC5B
0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47 4
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs861528
XRCC3 ; ZFYVE21
0.925 0.080 14 103716661 intron variant C/T snv 0.17 2
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs843706
ACYP2 ; TSPYL6
0.807 0.160 2 54253232 3 prime UTR variant C/A snv 0.42 6
rs830083
DDB2
0.807 0.120 11 47232500 intron variant G/A;C;T snv 6
rs828907
XRCC5
0.827 0.160 2 216108009 intron variant G/T snv 0.37 6
rs822395
ADIPOQ
0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs8193
CD44
0.925 0.080 11 35229771 3 prime UTR variant C/T snv 0.29 4
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs8126
TNFAIP2
0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs8113645
TINCR
0.925 0.080 19 5561065 3 prime UTR variant A/G;T snv 2
rs8111742
MIRLET7E ; MIR99B ; SPACA6 ; SPACA6P-AS ; MIR125A
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30 4
rs804270
NEIL2
0.882 0.080 8 11770112 5 prime UTR variant G/C;T snv 3
rs80358829
BRCA2
0.827 0.120 13 32340327 missense variant C/T snv 6
rs80142782
ASH1L
1.000 0.080 1 155515236 intron variant T/C snv 2.9E-03 1
rs799917
BRCA1
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs79777494
MUTYH
0.882 0.120 1 45334495 missense variant G/A snv 1.1E-03 4.9E-04 3
rs7975
GSTZ1
0.763 0.320 14 77326864 stop gained G/A;C;T snv 0.31 0.32 9
rs7972
GSTZ1
0.851 0.120 14 77326894 missense variant G/A snv 7.0E-02 7.0E-02 4
rs79402775
ATF2 ; MIR933
0.827 0.200 2 175167648 mature miRNA variant G/A;T snv 4.4E-02; 1.0E-05 5
rs79071878
LOC105379176 ; IL4
0.827 0.240 5 132680652 intron variant ATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAAT/- del 7
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93