Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs16260
CDH1
0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 19
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs12532
MSX1
0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs522616
MMP3
0.763 0.320 11 102844317 upstream gene variant T/C snv 0.23 10
rs587777450
PIEZO2
0.790 0.320 18 10671729 missense variant C/T snv 9
rs104894110
FOXE1 ; PTCSC2
0.776 0.280 9 97854108 missense variant C/T snv 8
rs104893810
TGFBR2
0.790 0.360 3 30691477 missense variant C/T snv 7
rs7650466
EPHA3
0.851 0.200 3 89481208 3 prime UTR variant C/T snv 0.23 7
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs4783099
CRISPLD2
0.827 0.200 16 84907723 3 prime UTR variant C/T snv 0.37 6
rs10130587
BMP4
0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
rs11466285
TGFA
0.851 0.200 2 70450307 3 prime UTR variant A/C;G snv 5
rs13041247
LOC102724968
0.851 0.200 20 40640434 regulatory region variant T/C snv 0.36 5
rs1474322770
NKX2-1 ; NKX2-1-AS1 ; SFTA3
0.827 0.240 14 36519251 missense variant G/A snv 5
rs2124459
CBS
0.827 0.200 21 43055604 3 prime UTR variant T/C snv 0.36 5
rs2239907
SARM1 ; SLC46A1
0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs2326398
CRISPLD2
0.827 0.200 16 84869111 intron variant A/G snv 0.37 5
rs3771523
TGFA
0.851 0.200 2 70450336 3 prime UTR variant C/T snv 0.14 5
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4