Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs26318
COMMD10
0.925 0.040 5 116352208 intron variant C/T snv 0.99 3
rs324899
LINC00461
0.925 0.040 5 88619764 intron variant A/G snv 0.97 2
rs643410
TMEM245
1.000 0.040 9 109037283 intron variant A/C snv 0.93 1
rs133047
MRTFA
1.000 0.040 22 40631815 intron variant T/C snv 0.93 3
rs7752195
CARMIL1 ; CMAHP
1.000 0.040 6 25418866 intron variant T/C snv 0.93 2
rs7732249
PDE4D
1.000 0.040 5 60070442 intron variant C/T snv 0.92 1
rs10750489
NTM
1.000 0.040 11 131786445 intron variant C/G;T snv 0.91 1
rs227932
CLK2P1
1.000 0.040 7 23584856 downstream gene variant A/G snv 0.90 1
rs1490191 1.000 0.040 1 151944275 upstream gene variant C/A snv 0.90 2
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs1521470
ADCY1
0.925 0.040 7 45607253 intron variant A/G snv 0.89 2
rs760816 1.000 0.040 1 4796871 downstream gene variant A/G snv 0.87 1
rs2962250 1.000 0.040 5 51094157 intergenic variant G/A snv 0.86 1
rs210152
GGNBP1
1.000 0.040 6 33547743 intron variant G/A snv 0.86 1
rs1198589 1.000 0.040 1 98084855 intergenic variant T/C snv 0.85 1
rs4968678
SCN4A ; LOC105371858
1.000 0.040 17 63966848 intron variant A/G snv 0.85 1
rs4234898 1.000 0.040 4 156077389 intergenic variant T/C snv 0.85 1
rs10744422
HIP1R
1.000 0.040 12 122852242 intron variant T/C snv 0.85 1
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs2868985
LOC105374690 ; MIR217HG
1.000 0.040 2 55964335 intron variant G/A snv 0.84 1
rs281768
MAIP1
1.000 0.040 2 199960517 intron variant A/T snv 0.84 2
rs7319102
PCDH17
1.000 0.040 13 57678667 intron variant G/A snv 0.83 3
rs2144683
LOC101928354
1.000 0.040 6 14717284 intron variant C/G snv 0.83 2
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs3845702
CWC22
1.000 0.040 2 179983761 intron variant C/A snv 0.83 1