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: rs886039769
rs886039769
10 0.807 0.160 9 124500686 missense variant G/A snv 0.020 1.000 2 2017 2019
dbSNP: rs1173716957
rs1173716957
3 1.000 0.120 1 210464508 missense variant G/T snv 1.4E-05 0.010 1.000 1 2014 2014
dbSNP: rs121913494
rs121913494
7 0.827 0.240 20 58909541 missense variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1478477850
rs1478477850
1 9 124500181 missense variant G/A;T snv 4.1E-06; 4.1E-06 0.010 1.000 1 2019 2019
dbSNP: rs200755477
rs200755477
3 0.925 0.120 22 43528870 missense variant G/A snv 1.2E-04 1.0E-04 0.010 1.000 1 2019 2019
dbSNP: rs2073043
rs2073043
1 X 150473747 missense variant A/G snv 0.11 0.10 0.010 1.000 1 2012 2012
dbSNP: rs41313406
rs41313406
1 X 150470648 missense variant C/T snv 8.3E-02 8.3E-02 0.010 1.000 1 2012 2012
dbSNP: rs62641609
rs62641609
1 X 150470614 missense variant C/A snv 5.4E-03 1.9E-02 0.010 1.000 1 2012 2012
dbSNP: rs748162844
rs748162844
1 X 30308585 missense variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs9332964
rs9332964
10 0.763 0.240 2 31529325 missense variant C/T snv 4.7E-04 1.6E-04 0.010 1.000 1 2019 2019