Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115510139
COL6A3
0.827 0.120 2 237331726 intron variant A/T snv 0.60 6
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs315919
IL1RN
0.851 0.120 2 113118636 intron variant T/G snv 0.55 5
rs3181052
IL1RN
0.851 0.120 2 113128472 intron variant G/A snv 0.16 5
rs1595066
ERBB4
0.882 0.080 2 211377000 3 prime UTR variant C/T snv 0.28 4
rs16845990
ERBB4
0.882 0.080 2 211378286 3 prime UTR variant T/A;C snv 4
rs2244438
TRAK2
0.882 0.080 2 201387816 missense variant G/A;T snv 0.29; 4.0E-06 4
rs3738894
PRKCE
0.882 0.080 2 46187030 3 prime UTR variant G/A snv 1.1E-02 4
rs6720283
COL6A3
0.882 0.120 2 237401239 intron variant G/A snv 0.31 4
rs7436
COL6A3
0.925 0.080 2 237324168 3 prime UTR variant T/A snv 0.10 3
rs1430055 2 16499521 intergenic variant G/A snv 0.61 2
rs2252641
TEX41 ; LOC100505498
1.000 0.040 2 145043894 non coding transcript exon variant T/C;G snv 0.58 2
rs4851005
IL18R1
2 102395092 intron variant C/T snv 0.29 2
rs7578456 1.000 0.080 2 201370625 intergenic variant A/G snv 0.57 2
rs10186527
FLACC1
2 201335852 intron variant C/T snv 0.54 1
rs10191793
ST6GAL2
2 106809420 intron variant A/G snv 0.21 1
rs10197246
FLACC1
2 201340018 intron variant T/C snv 0.72 1
rs10201587
FLACC1
2 201338068 intron variant A/G snv 0.47 1
rs10454127
FLACC1
2 201347651 intron variant G/A;T snv 1
rs11898821
FLACC1
2 201334965 intron variant T/C snv 0.46 1
rs2080304
FLACC1
2 201321699 intron variant G/C snv 0.59 1
rs2110690
FLACC1
2 201320409 intron variant A/G snv 0.42 1
rs2349073
FLACC1
2 201322263 intron variant C/A snv 0.75 1
rs4283388 2 172374994 downstream gene variant C/T snv 0.33 1
rs6435079
FLACC1
2 201335608 intron variant C/G;T snv 1