Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1490176
SORCS3
1.000 0.040 10 104800467 intron variant T/A;G snv 2
rs17487484
DCC
1.000 0.040 18 53196913 intron variant T/A;G snv 2
rs1782179 1.000 0.040 14 41224737 intergenic variant T/A;C snv 2
rs182087934 2 183742707 intergenic variant G/A snv 2
rs1875560
DCC
1.000 0.040 18 53434318 intron variant A/C;G snv 2
rs200312707
CDH8
1.000 0.040 16 62031776 intron variant TA/- del 2
rs2278609
PLCL2 ; LOC105376972
1.000 0.040 3 16882947 intron variant C/A;G;T snv 2
rs2688708 1.000 0.040 11 55073194 intergenic variant C/G;T snv 2
rs297346
SOX6
1.000 0.040 11 16334225 intron variant A/G;T snv 2
rs34807503 1.000 0.040 12 51525350 intergenic variant ATTTATTT/-;ATTT;ATTTATTTATTT delins 2
rs35909029
LINC02210-CRHR1
1.000 0.040 17 45774132 intron variant T/A;C;G snv 2
rs3819325
UBA7 ; MIR5193
1.000 0.040 3 49806290 non coding transcript exon variant T/C;G snv 0.38; 7.9E-04 2
rs60393230
LOC107987122
1.000 0.040 9 119893005 intergenic variant A/G;T snv 2
rs6074013
NCOA5
1.000 0.040 20 46080900 intron variant C/A;G;T snv 2
rs62183032
ERBB4
1.000 0.040 2 211774137 intron variant A/G;T snv 2
rs6475417
SLC24A2
9 20212043 intergenic variant A/G;T snv 2
rs6661750
PDE4B
1 66081201 intron variant A/G;T snv 2
rs6779928 1.000 0.040 3 16717777 intergenic variant G/A;C snv 2
rs7128325
C11orf49
1.000 0.040 11 47025003 intron variant G/A;C;T snv 2
rs7714426
PRR16
1.000 0.040 5 120683373 intron variant C/A;G;T snv 2
rs9586
KLHDC8B
1.000 0.040 3 49176204 3 prime UTR variant C/G;T snv 2
rs9930139
RBFOX1
1.000 0.040 16 7239569 intron variant A/C;T snv 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs717454
REV1
1.000 0.040 2 99406310 non coding transcript exon variant T/C;G snv 0.44; 8.2E-06 1