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: rs1057519721
rs1057519721
4 0.882 0.120 9 5078360 missense variant A/G snv 0.700 1.000 4 2008 2012
dbSNP: rs1057519722
rs1057519722
1 1.000 0.120 9 5078361 missense variant G/C snv 4.0E-06 0.700 1.000 4 2008 2012
dbSNP: rs1057519723
rs1057519723
2 0.925 0.120 9 5078362 missense variant A/C;G;T snv 0.700 1.000 4 2008 2012
dbSNP: rs1057519743
rs1057519743
6 0.827 0.120 Y 1196852 missense variant A/C snv 0.700 1.000 4 2010 2012
dbSNP: rs1057519753
rs1057519753
9 0.763 0.120 1 64846664 missense variant C/A snv 0.700 1.000 4 2009 2011
dbSNP: rs121913459
rs121913459
25 0.672 0.160 9 130872896 missense variant C/T snv 0.700 1.000 3 2002 2014
dbSNP: rs121913461
rs121913461
5 0.851 0.120 9 130862970 missense variant T/C snv 0.700 1.000 3 2002 2014
dbSNP: rs1057519759
rs1057519759
1 1.000 0.120 5 35873495 missense variant A/T snv 0.700 1.000 2 2012 2012
dbSNP: rs1057519897
rs1057519897
6 0.807 0.240 8 38414788 missense variant C/G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs151047872
rs151047872
1 1.000 0.120 1 64846699 missense variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs869312953
rs869312953
5 0.851 0.120 1 64846735 missense variant G/T snv 0.700 1.000 1 2010 2010
dbSNP: rs869320694
rs869320694
16 0.742 0.520 8 38414790 missense variant T/C snv 0.700 1.000 1 2016 2016