Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7993214
COG6
0.925 0.040 13 39776775 intron variant T/C;G snv 2
rs6701216
LCE1C
0.925 0.040 1 152806050 intron variant C/T snv 0.21 2
rs3803369
TNFAIP8L3 ; MIR4713HG
0.925 0.040 15 51083632 intron variant T/A;C snv 2