Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs16847897
LRRC31
0.851 0.320 3 169850328 intron variant G/A;C snv 4
rs121912985
DSPP
0.925 0.080 4 87612186 stop gained C/A;T snv 2
rs2630578
BICD1
1.000 0.040 12 32152853 intron variant G/C snv 0.14 1