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: rs121908464
rs121908464
1 1.000 0.080 16 57661707 missense variant C/T snv 8.1E-06 2.8E-05 0.810 1.000 6 2004 2017
dbSNP: rs121908462
rs121908462
1 1.000 0.080 16 57651247 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.800 1.000 6 2004 2014
dbSNP: rs121908463
rs121908463
1 1.000 0.080 16 57656244 missense variant T/A snv 0.800 1.000 6 2004 2014
dbSNP: rs121908465
rs121908465
1 1.000 0.080 16 57651407 missense variant G/C snv 0.800 1.000 6 2004 2014
dbSNP: rs121908466
rs121908466
1 1.000 0.080 16 57651398 missense variant A/G snv 0.800 1.000 6 2004 2014
dbSNP: rs556518689
rs556518689
1 1.000 0.080 16 57659594 missense variant G/A snv 4.0E-06 7.0E-06 0.710 1.000 6 2004 2014
dbSNP: rs764367185
rs764367185
1 1.000 0.080 16 57651248 missense variant G/A snv 4.0E-06 1.4E-05 0.700 1.000 6 2004 2014