Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4482537 0.925 0.040 2 48825116 intron variant C/T snv 0.52 2
rs2295334
C6orf223 ; LOC101929705
0.925 0.040 6 44003090 synonymous variant G/A snv 5.0E-02 3.9E-02 2
rs75165563
EXOC5
0.925 0.040 14 57220928 intron variant A/C snv 4.5E-04 2
rs10507047
FGD6
0.925 0.040 12 95210514 missense variant T/C snv 0.12 0.11 2
rs8002574
LHFPL6 ; LOC105370170
0.925 0.040 13 39504403 intron variant C/T snv 0.13 2
rs28368872 0.882 0.040 16 10491493 upstream gene variant G/A snv 0.22 3
rs2284665
HTRA1
0.882 0.040 10 122467114 intron variant G/A;T snv 3
rs12661281
SLC44A4 ; CYP21A2
0.882 0.040 6 31874821 missense variant T/A snv 0.15 0.11 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