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: rs104894555
rs104894555
1 1.000 0.080 17 14102205 missense variant C/A snv 0.800 1.000 3 2000 2016
dbSNP: rs104894556
rs104894556
2 1.000 0.080 17 14159926 missense variant C/G;T snv 1.2E-05 0.800 1.000 3 2000 2016
dbSNP: rs104894557
rs104894557
2 0.925 0.120 17 14206888 missense variant A/G;T snv 8.0E-05 0.800 1.000 3 2000 2016
dbSNP: rs104894560
rs104894560
1 1.000 0.080 17 14102230 missense variant C/A snv 4.0E-06 0.800 1.000 3 2000 2016
dbSNP: rs773079584
rs773079584
1 1.000 0.080 17 14207140 missense variant C/G;T snv 4.0E-06; 4.0E-06; 1.6E-05 0.700 1.000 3 2000 2016
dbSNP: rs753048807
rs753048807
1 1.000 0.080 17 14192155 missense variant G/A snv 7.0E-06 0.700 0