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: rs28940306
rs28940306
1 1.000 0.120 19 50271424 missense variant C/T snv 4.3E-06; 8.6E-06 0.800 1.000 2 2004 2005
dbSNP: rs28940307
rs28940307
1 1.000 0.120 19 50259210 missense variant C/A snv 0.800 1.000 2 2004 2005
dbSNP: rs367588704
rs367588704
1 1.000 0.120 19 50268305 missense variant G/A snv 1.5E-05 7.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs119103279
rs119103279
1 1.000 0.120 19 50210385 stop gained C/A;T snv 0.700 0
dbSNP: rs119103280
rs119103280
1 1.000 0.120 19 50244277 missense variant G/T snv 3.0E-03 3.0E-03 0.700 0
dbSNP: rs119103281
rs119103281
1 1.000 0.120 19 50210724 missense variant C/T snv 0.700 0