Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117496742
YAP1
1.000 0.120 11 102208982 intron variant G/A;T snv 1.3E-02 1
rs522616
MMP3
0.763 0.320 11 102844317 upstream gene variant T/C snv 0.23 10
rs11624283 0.882 0.200 14 105124634 downstream gene variant A/G snv 0.13 3
rs587777450
PIEZO2
0.790 0.320 18 10671729 missense variant C/T snv 9
rs197204
MCUB
0.851 0.200 4 109576918 intron variant C/G snv 0.52 4
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs11066150
NAA25
0.925 0.120 12 112080999 intron variant G/A snv 1.3E-02 2
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs7078160
SHTN1
0.851 0.120 10 117068049 intron variant G/A snv 0.19 4
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs10886040
SHTN1
0.882 0.120 10 117086783 intron variant C/G snv 0.20 3
rs6585429
VAX1
0.925 0.120 10 117133720 3 prime UTR variant A/G snv 0.68 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs7554547 0.925 0.120 1 11913831 non coding transcript exon variant A/G;T snv 2
rs150382487
LINC02476
1.000 0.120 7 119500548 intron variant T/A snv 2.4E-03 1
rs188681640
LINC02476
1.000 0.120 7 119506105 intron variant A/G snv 2.4E-03 1
rs182830500
LINC02476
1.000 0.120 7 119521299 intron variant T/C snv 2.6E-03 1
rs143238378
LINC02476
1.000 0.120 7 119626216 intron variant G/A;T snv 1
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs7692299
LINC01091
0.925 0.120 4 123789429 intron variant C/T snv 0.15 2
rs908822 0.925 0.120 4 123985102 regulatory region variant C/A;T snv 2
rs72728734
CCDC26
0.882 0.120 8 128921474 intron variant A/G snv 0.13 3
rs7017252
CCDC26
0.925 0.120 8 128938598 intron variant C/T snv 0.32 2
rs55658222
LINC00976 ; CCDC26
0.925 0.120 8 128963890 intron variant G/A snv 0.14 2