Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41291957
CARMN ; MIR145 ; MIR143
0.882 0.200 5 149428827 intron variant G/A snv 0.12 7
rs4705343
MIR143 ; CARMN
0.790 0.240 5 149428518 non coding transcript exon variant T/C snv 0.14 7
rs353293
CARMN ; MIR143
0.851 0.160 5 149427663 non coding transcript exon variant C/T snv 0.33 4
rs4705342
MIR143 ; CARMN
0.851 0.160 5 149428408 non coding transcript exon variant T/C;G snv 4
rs353292
MIR143 ; CARMN
0.882 0.080 5 149428245 non coding transcript exon variant G/A snv 0.35 3
rs17723799
MIR143 ; CARMN
1.000 0.120 5 149427514 non coding transcript exon variant C/T snv 9.9E-02 1