Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs722782 1.000 0.040 8 566479 intergenic variant A/C;T snv 1
rs749856572
RAD51B
1.000 0.040 14 67835182 stop gained G/A;T snv 4.0E-06 1
rs1789110 0.925 0.040 18 77147088 regulatory region variant C/A snv 0.63 2
rs2842992 0.925 0.040 6 159650127 intron variant G/A snv 0.73 2
rs1253615192
HTRA1 ; LOC105378525
0.925 0.040 10 122461959 missense variant C/G snv 7.0E-06 2
rs1460548929
PRKCSH
0.925 0.040 19 11442432 missense variant A/G snv 4.0E-06 2
rs151207349
PRKCSH
0.925 0.040 19 11441343 missense variant C/T snv 7.0E-04 5.7E-04 2
rs28368872 0.882 0.040 16 10491493 upstream gene variant G/A snv 0.22 3
rs58978565
TNR
0.882 0.040 1 175376466 intron variant -/AGAGT ins 0.37 3
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4
rs62247658
ADAMTS9-AS2
0.851 0.040 3 64729479 intron variant C/T snv 0.42 4
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs3750846
ARMS2 ; LOC105378525
0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs9564692
B3GLCT
0.851 0.040 13 31247103 splice region variant C/T snv 0.40 0.36 4
rs5817082
CETP
0.851 0.040 16 56963437 intron variant -/A delins 4
rs35292876
CFH
0.851 0.040 1 196737512 synonymous variant C/T snv 1.0E-02 8.6E-03 4
rs191281603
CFHR5
0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4
rs67538026
CNN2
0.851 0.040 19 1031439 intron variant C/T snv 0.37 4
rs11884770
COL4A3 ; MFF-DT
0.851 0.040 2 227222204 intron variant T/A;C snv 4
rs55975637
COL8A1
0.851 0.040 3 99701009 intron variant G/A;T snv 4