Disease: Nuclear non-senile cataract
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11574311
WRN
0.776 0.160 8 31119144 intron variant T/C snv 0.16 8
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