Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3020450
ESR2
0.807 0.200 14 64301584 splice region variant C/A;T snv 10
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 9
rs12964965
DLGAP1
0.925 0.080 18 3520557 intron variant T/C snv 0.33 2
rs2813544
ESR1
0.925 0.080 6 152104447 intron variant A/G snv 0.22 2
rs763744183
LOC102725238 ; CAVIN1
0.925 0.080 17 42422922 missense variant T/A snv 1.2E-05 2