Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs35947132
PRF1
0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 10
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs768713502
AMH ; MIR4321
0.882 0.120 19 2250752 missense variant G/A;T snv 7.6E-06; 1.5E-05 5
rs587777840
NLRC4
0.882 0.080 2 32250855 missense variant T/A snv 4