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: rs121908664
rs121908664
1 1.000 0.120 11 68389949 missense variant G/A snv 0.800 1.000 5 2001 2008
dbSNP: rs121908665
rs121908665
1 1.000 0.120 11 68403606 missense variant C/T snv 0.800 1.000 5 2001 2008
dbSNP: rs1219101402
rs1219101402
1 1.000 0.120 11 68365607 missense variant C/T snv 7.0E-06 0.700 1.000 5 2001 2008
dbSNP: rs201320326
rs201320326
1 1.000 0.120 11 68386499 missense variant C/A;T snv 2.2E-04 0.700 1.000 5 2001 2008
dbSNP: rs377258285
rs377258285
1 1.000 0.120 11 68425202 missense variant C/T snv 5.6E-05 6.3E-05 0.700 1.000 5 2001 2008
dbSNP: rs397514665
rs397514665
1 1.000 0.120 11 68363791 missense variant C/T snv 1.2E-05 0.800 1.000 5 2001 2008
dbSNP: rs545508982
rs545508982
1 1.000 0.120 11 68389980 stop gained G/A;T snv 4.0E-06; 8.0E-06 0.700 1.000 5 2001 2008
dbSNP: rs760548029
rs760548029
1 1.000 0.120 11 68357768 missense variant G/A snv 4.0E-06 7.0E-06 0.700 1.000 5 2001 2008
dbSNP: rs80358313
rs80358313
3 0.882 0.160 11 68406550 missense variant G/A;C;T snv 1.2E-05; 1.2E-05; 3.2E-05 0.700 1.000 5 2001 2008
dbSNP: rs866606166
rs866606166
1 1.000 0.120 11 68386678 missense variant G/A snv 7.0E-06 0.700 1.000 5 2001 2008
dbSNP: rs121908668
rs121908668
5 0.882 0.240 11 68357673 missense variant G/T snv 0.010 1.000 1 2017 2017
dbSNP: rs121908674
rs121908674
3 0.882 0.160 11 68410076 missense variant C/G;T snv 0.010 1.000 1 2015 2015