Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555640521
LAMA1
0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs10034259
LINC02503
1.000 0.040 4 104012596 intron variant A/C snv 0.19 1
rs12260436
CNNM2
1.000 0.040 10 102981357 intron variant A/C snv 0.29 1
rs1330745 1.000 0.040 13 58585815 intergenic variant A/C snv 0.15 1
rs34569203 1.000 0.040 6 27186205 intergenic variant A/C snv 0.14 1
rs62551581
LOC105375975
1.000 0.040 9 11610677 intergenic variant A/C snv 0.15 1
rs6807666
CADM2
1.000 0.040 3 85545278 intron variant A/C snv 0.59 1
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs12923795
RBFOX1
1.000 0.040 16 7612705 intron variant A/C;G snv 1
rs488359
LOC107984941
1.000 0.040 1 36698055 intergenic variant A/C;G snv 1
rs9936170
ZCCHC14
1.000 0.040 16 87477955 intron variant A/C;G snv 1
rs1890184
CNNM2
1.000 0.040 10 102988702 intron variant A/C;T snv 1
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 4
rs4434138
STAB1
1.000 0.040 3 52522874 missense variant A/G snv 8.0E-06; 0.44 0.39 2
rs80533 1.000 0.040 22 40689965 intergenic variant A/G snv 0.81 2
rs9829032
CADM2
0.925 0.080 3 85634450 intron variant A/G snv 0.41 2
rs13282237
TSNARE1
1.000 0.040 8 142244830 intron variant A/G snv 0.55 1
rs1368748
CADM2
1.000 0.040 3 85363180 intron variant A/G snv 0.50 1
rs17196295
SATB2
1.000 0.040 2 199287475 intron variant A/G snv 0.21 1
rs28639817
SGCZ
1.000 0.040 8 14293898 intron variant A/G snv 0.15 1
rs391236 1.000 0.040 5 103342372 intergenic variant A/G snv 0.24 1
rs3988211
WBP2
1.000 0.040 17 75850024 intron variant A/G snv 0.95 1