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: rs121909084
rs121909084
ROR2
1 1.000 0.120 9 91737463 missense variant G/A snv 4.0E-06 0.800 1.000 2 2000 2000
dbSNP: rs121909083
rs121909083
ROR2
1 1.000 0.120 9 91724990 stop gained G/A snv 4.0E-06 0.700 1.000 1 2000 2000
dbSNP: rs267607016
rs267607016
ROR2
3 0.882 0.120 9 91726603 stop gained G/A snv 4.0E-06 1.4E-05 0.700 1.000 1 2009 2009
dbSNP: rs121909085
rs121909085
ROR2
1 1.000 0.120 9 91724334 stop gained C/T snv 0.700 0
dbSNP: rs121909086
rs121909086
ROR2
1 1.000 0.120 9 91737400 stop gained G/A;T snv 4.0E-06 0.700 0
dbSNP: rs121909087
rs121909087
ROR2
1 1.000 0.120 9 91757380 stop gained G/A snv 0.700 0
dbSNP: rs199975149
rs199975149
ROR2
1 1.000 0.120 9 91737448 missense variant G/A snv 8.0E-06 2.1E-05 0.700 0
dbSNP: rs863223291
rs863223291
ROR2
1 1.000 0.120 9 91724551 frameshift variant CTTGTAG/- delins 0.700 0