Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs6220
LINC02456 ; HELLPAR ; IGF1
0.925 0.080 12 102400737 3 prime UTR variant G/A snv 0.67 4
rs1520220
LINC02456 ; IGF1
0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs2195239
LINC02456 ; IGF1
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28 7
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs1598859
NFKB1
0.925 0.080 4 102585287 intron variant T/C snv 0.34 4
rs35866072
MMP8
0.716 0.360 11 102713373 missense variant T/G snv 6.0E-02 9.8E-02 17
rs34009635
MMP8
0.716 0.360 11 102713445 missense variant A/G snv 2.5E-03 6.2E-04 17
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs1940475
MMP8
1.000 0.040 11 102722517 missense variant T/C;G snv 0.54 4
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs751402
ERCC5 ; BIVM-ERCC5
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs2296147
BIVM-ERCC5 ; ERCC5
0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs2227869
ERCC5 ; BIVM-ERCC5
0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9
rs2075356
GHRL ; GHRLOS
0.882 0.160 3 10287125 non coding transcript exon variant T/C snv 8.3E-02 5
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52