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: rs387906608
rs387906608
1 1.000 0.143 21 46132118 missense variant C/A,G,T snp 5.2E-06; 2.1E-05 0.710 1.000 2 2006 2010
dbSNP: rs121912938
rs121912938
1 1.000 0.143 21 45989129 missense variant G/A snp 0.700 3 2005 2007
dbSNP: rs112638391
rs112638391
1 1.000 0.143 2 237374900 missense variant C/T snp 3.0E-03 8.9E-04 0.700 1 2006 2006
dbSNP: rs267606746
rs267606746
1 1.000 0.143 21 45989120 missense variant G/A snp 0.700 1 2006 2006
dbSNP: rs267606748
rs267606748
1 1.000 0.143 21 46115917 missense variant G/A snp 0.700 1 2006 2006
dbSNP: rs267606749
rs267606749
1 1.000 0.143 21 46121590 missense variant G/A snp 2.4E-05 0.700 1 2006 2006
dbSNP: rs75120695
rs75120695
1 1.000 0.143 21 46126166 missense variant G/A,C snp 4.4E-03 3.2E-03 0.700 1 2006 2006
dbSNP: rs778940391
rs778940391
1 1.000 0.143 2 237367167 missense variant C/T snp 1.6E-04 2.2E-04 0.700 1 2006 2006
dbSNP: rs80272723
rs80272723
1 1.000 0.143 2 237371833 missense variant C/A,T snp 1.0E-02 3.2E-05; 5.9E-03 0.700 1 2006 2006
dbSNP: rs121912939
rs121912939
2 0.923 0.143 21 45989617 missense variant G/A,C snp 0.700 0
dbSNP: rs387906607
rs387906607
1 1.000 0.143 21 46125518 missense variant G/A snp 4.0E-06 3.2E-05 0.010 1.000 1 2010 2010