Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs141746753 1.000 0.040 8 56934154 intergenic variant C/T snv 3.1E-03 3
rs1994321 1.000 0.040 11 12065766 upstream gene variant G/T snv 0.33 3
rs2979204 0.925 0.040 8 8441347 regulatory region variant T/C snv 0.34 3
rs4761545 0.925 0.040 12 94032692 regulatory region variant G/T snv 0.56 3
rs73720034 1.000 0.040 7 125794995 intergenic variant T/C snv 7.2E-02 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs7828021 0.925 0.040 8 49727454 intergenic variant C/G;T snv 3
rs138472420
BICRA
1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs11082011
CELF4
0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs150175932
DCLK2
1.000 0.040 4 150101495 intron variant T/C snv 1.6E-02 3
rs73788091
FSTL4 ; MIR1289-2
1.000 0.040 5 133429517 intron variant C/T snv 0.10 3
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs80164876
LOC105374732 ; EGFLAM
1.000 0.040 5 38464142 3 prime UTR variant A/G snv 1.9E-02 3
rs55679149
LOC105378841
0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs35863382
PPP4R3A
1.000 0.040 14 91472532 intron variant C/T snv 6.0E-02 3
rs7189979
SNX29
0.925 0.040 16 12536330 intron variant A/C;G;T snv 3
rs352759
TUSC3
0.925 0.040 8 15742205 intron variant T/A snv 3