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: rs121964863
rs121964863
DDR2
1 1.000 0.120 1 162776341 missense variant C/T snv 0.810 1.000 3 2009 2016
dbSNP: rs121964865
rs121964865
DDR2
1 1.000 0.120 1 162776225 missense variant C/A;T snv 4.0E-06 0.810 1.000 3 2009 2016
dbSNP: rs397514747
rs397514747
DDR2
1 1.000 0.120 1 162754775 missense variant G/A snv 0.810 1.000 3 2009 2016
dbSNP: rs121964864
rs121964864
DDR2
1 1.000 0.120 1 162776264 missense variant T/G snv 0.800 1.000 3 2009 2016
dbSNP: rs1293840159
rs1293840159
ITGA2
1 1.000 0.120 5 53070250 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2010 2010