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: rs113994099
rs113994099
10 0.827 0.240 15 89320883 missense variant T/C snv 0.020 1.000 2 2007 2007
dbSNP: rs121918055
rs121918055
2 0.925 0.200 15 89326965 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs1463467386
rs1463467386
1 1.000 0.200 15 89327059 missense variant T/C;G snv 4.0E-06 1.4E-05 0.010 1.000 1 2008 2008