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: rs121908336
rs121908336
1 1.000 0.040 10 86706669 missense variant C/G;T snv 4.0E-06; 2.8E-04 0.800 1.000 2 2003 2004
dbSNP: rs121908337
rs121908337
1 1.000 0.040 10 86681731 missense variant C/T snv 1.6E-05 7.0E-06 0.800 1.000 2 2003 2004
dbSNP: rs45487699
rs45487699
1 1.000 0.040 10 86681680 missense variant C/T snv 6.5E-04 5.0E-04 0.800 0
dbSNP: rs45514002
rs45514002
1 1.000 0.040 10 86726175 missense variant G/A snv 1.1E-04 4.9E-05 0.700 0