Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs1864183
ATG10
0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs3759601
ATG2B
0.790 0.240 14 96311131 missense variant G/C snv 0.36 0.32 7
rs2230600
PTPN13
0.827 0.160 4 86769845 missense variant A/G snv 0.18 0.14 5
rs763015080
EDNRA
0.851 0.120 4 147539821 missense variant G/A snv 4.1E-06 4
rs35431622
KISS1
0.851 0.120 1 204190794 missense variant T/A;C snv 5.5E-05; 4.7E-02 4
rs1494961
HELQ
0.925 0.160 4 83453327 missense variant C/T snv 0.56 0.60 3