Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs11574311
WRN
0.776 0.160 8 31119144 intron variant T/C snv 0.16 8
rs74315439
CRYAA ; LOC107987300
0.790 0.200 21 43172104 missense variant C/A;T snv 7
rs2725338
WRN
0.790 0.120 8 31042501 intron variant G/A snv 7.6E-02 7
rs1063147
BLM
0.807 0.120 15 90811275 synonymous variant C/T snv 0.15 6
rs2725383
WRN
0.807 0.120 8 31075099 intron variant C/G snv 0.76 6
rs4733220
WRN
0.807 0.120 8 31043374 intron variant A/G snv 0.50 6
rs397515624
CRYAA ; LOC107987300
0.851 0.040 21 43169133 missense variant C/T snv 4.0E-06 4
rs121434643
GJA8
0.851 0.200 1 147908094 missense variant G/A;C snv 4
rs202235939
CD48
0.925 0.040 1 160679109 missense variant C/G snv 3.3E-04 2.4E-04 2
rs1198082657
SLC11A2
0.925 0.040 12 50992197 missense variant C/T snv 7.0E-06 2