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: rs121918154
rs121918154
PROC ; LOC105373608
2 1.000 0.080 2 127428374 missense variant C/A;T snv 4.0E-06; 2.0E-05 0.700 1.000 1 2019 2019
dbSNP: rs1553424043
rs1553424043
PROC ; MIR4783
3 0.925 0.120 2 127423123 missense variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs369504169
rs369504169
PROC
3 0.925 0.120 2 127421337 missense variant G/A snv 8.0E-06 7.0E-06 0.700 1.000 1 2019 2019