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: rs72552758
rs72552758
1 0.882 0.200 6 32040919 missense variant G/A snv 1.5E-05 3.5E-05 0.710 1.000 20 1985 2016
dbSNP: rs747079101
rs747079101
1 0.925 0.240 6 32040491 missense variant G/A;C snv 3.2E-05 0.700 1.000 20 1985 2016
dbSNP: rs755020999
rs755020999
1 1.000 0.200 6 32006687 non coding transcript exon variant T/C snv 4.2E-06 0.700 1.000 20 1985 2016
dbSNP: rs759736443
rs759736443
1 0.882 0.240 6 32041096 missense variant C/T snv 2.1E-04; 2.7E-05 7.0E-06 0.700 1.000 20 1985 2016
dbSNP: rs760216630
rs760216630
1 0.925 0.200 6 32040530 missense variant G/A snv 0.700 1.000 20 1985 2016
dbSNP: rs772317717
rs772317717
1 1.000 0.200 6 32039443 missense variant G/A snv 0.700 1.000 20 1985 2016
dbSNP: rs7769409
rs7769409
1 0.882 0.200 6 32040535 missense variant C/T snv 7.0E-05 0.810 1.000 20 1985 2016
dbSNP: rs776989258
rs776989258
1 0.807 0.280 6 32041093 missense variant C/G;T snv 5.5E-04 0.820 1.000 20 1985 2016
dbSNP: rs781074931
rs781074931
1 1.000 0.200 6 32040574 missense variant C/A;T snv 4.1E-06; 6.1E-05 0.700 1.000 20 1985 2016
dbSNP: rs200005406
rs200005406
1 0.851 0.200 6 32041097 missense variant G/A;C snv 8.8E-06; 3.3E-04 0.710 1.000 0 1993 1993
dbSNP: rs9378252
rs9378252
1 0.882 0.200 6 32038610 missense variant A/G;T snv 4.4E-02 0.710 1.000 0 2008 2008