Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33 6
rs8068318
TBX2
17 61406405 non coding transcript exon variant C/T snv 0.56 6
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 5
rs10994860
A1CF
0.925 0.120 10 50885664 5 prime UTR variant C/T snv 0.19 5
rs7422339
CPS1
1.000 0.080 2 210675783 missense variant C/A snv 5
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 5
rs143709408
KCNQ1
0.882 0.200 11 2527999 missense variant C/T snv 1.6E-04 3.6E-04 5
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 5
rs10851885
NRG4
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18 5
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26 5
rs186459505
SFMBT1
0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 5
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs3812036
SLC34A1
0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 5
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 5
rs2453533 1.000 0.080 15 45349027 intergenic variant C/A snv 0.56 4
rs6465825 1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41 4
rs7123489 1.000 0.080 11 65756781 intron variant C/A snv 0.29 4
rs267738
CERS2
1.000 0.040 1 150968149 missense variant T/A;G snv 4.0E-06; 0.15 4
rs11959928
DAB2 ; C9
1.000 0.080 5 39397030 intron variant T/A snv 0.39 4
rs201874364
ETV5
1.000 0.040 3 186065822 missense variant C/A;T snv 4.0E-06; 7.2E-05 4