Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2842339
RAD51B
0.851 0.040 14 68520282 intron variant G/A snv 0.90 4
rs2842992 0.925 0.040 6 159650127 intron variant G/A snv 0.73 2
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1789110 0.925 0.040 18 77147088 regulatory region variant C/A snv 0.63 2
rs943080
LOC107986598
0.807 0.040 6 43858890 TF binding site variant C/T snv 0.61 6
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs61985136
RAD51B
0.851 0.040 14 68302482 intron variant C/T snv 0.52 4
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs62247658
ADAMTS9-AS2
0.851 0.040 3 64729479 intron variant C/T snv 0.42 4
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs67538026
CNN2
0.851 0.040 19 1031439 intron variant C/T snv 0.37 4
rs58978565
TNR
0.882 0.040 1 175376466 intron variant -/AGAGT ins 0.37 3
rs9564692
B3GLCT
0.851 0.040 13 31247103 splice region variant C/T snv 0.40 0.36 4
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs6565597
NPLOC4
0.851 0.040 17 81559795 intron variant C/T snv 0.30 4
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs5754227
SYN3
0.851 0.040 22 32709831 intron variant T/C snv 0.26 4
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27