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: rs1131692173
rs1131692173
EED
1 1.000 11 86268501 missense variant A/C;G snv 0.700 0
dbSNP: rs1131692174
rs1131692174
EED
1 1.000 11 86266128 missense variant C/T snv 0.700 0
dbSNP: rs1131692175
rs1131692175
EED
1 1.000 11 86268499 missense variant A/G snv 0.700 0
dbSNP: rs1131692176
rs1131692176
EED
1 1.000 11 86264244 missense variant G/C snv 0.700 0
dbSNP: rs1565706229
rs1565706229
EED ; MIR6755
18 0.851 0.120 11 86277110 missense variant T/C snv 0.700 0