Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555031372
rs1555031372
DPF2
3 0.925 0.280 11 65345981 missense variant G/T snv 0.800 1.000 1 2018 2018
dbSNP: rs1555031500
rs1555031500
DPF2
1 1.000 11 65346332 missense variant C/G snv 0.800 1.000 1 2018 2018
dbSNP: rs1555032044
rs1555032044
DPF2
1 1.000 11 65348869 missense variant A/G snv 0.800 1.000 1 2018 2018
dbSNP: rs1555032051
rs1555032051
DPF2
1 1.000 11 65348881 missense variant G/A snv 0.800 1.000 1 2018 2018
dbSNP: rs1555032074
rs1555032074
DPF2
1 1.000 11 65348932 splice donor variant G/A snv 0.700 0