Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3745453
ZSWIM4
1.000 0.080 19 13831407 3 prime UTR variant A/G snv 0.36 1
rs354033
ZNF767P
1.000 0.080 7 149592373 intron variant G/A snv 0.24 1
rs3745672
ZNF433-AS1 ; ZNF433
1.000 0.080 19 12035555 splice region variant T/C snv 4.0E-02 7.3E-02 1
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs1250542
ZMIZ1
1.000 0.080 10 79274913 intron variant G/A snv 0.32 1
rs1782645
ZMIZ1
1.000 0.080 10 79288854 intron variant C/A;T snv 1
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 4
rs1728785
ZFP90
0.925 0.120 16 68557327 intron variant A/C;T snv 0.77; 7.8E-06 2
rs1465788
ZFP36L1
0.925 0.160 14 68796882 upstream gene variant T/C snv 0.70 2
rs2236262
ZFP36L1
1.000 0.080 14 68794755 intron variant A/G snv 0.45 2
rs4902647
ZFP36L1
1.000 0.080 14 68787474 downstream gene variant C/A;T snv 1
rs733254
ZFAT
1.000 0.080 8 134626389 intron variant C/A;T snv 0.29 1
rs3735007
ZC3HAV1
1.000 0.080 7 139047751 missense variant G/A snv 0.50 0.56 1
rs6062314
ZBTB46
0.925 0.160 20 63778360 intron variant C/G;T snv 2
rs9846396
ZBTB38
1.000 0.080 3 141422126 intron variant C/T snv 0.50 2
rs207906
XRCC5
1.000 0.080 2 216148178 synonymous variant A/G snv 0.88 0.88 1
rs12149527
WWOX
1.000 0.080 16 79076699 intron variant C/T snv 0.36 1
rs7924357
WTAPP1
1.000 0.080 11 102757321 intron variant G/A snv 7.9E-02 1
rs1044165
VSIG4
1.000 0.080 X 66021884 3 prime UTR variant G/A snv 9.0E-02 1
rs2777899
VMP1
0.851 0.160 17 59755030 intron variant T/A;G snv 4
rs8070345
VMP1
1.000 0.080 17 59739396 intron variant T/C snv 0.41 1
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99