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: rs2279343
rs2279343
8 0.776 0.200 19 41009358 missense variant A/G snv 0.13 0.010 1.000 1 2011 2011
dbSNP: rs3745274
rs3745274
30 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 0.010 1.000 1 2011 2011
dbSNP: rs45459594
rs45459594
1 1.000 0.080 19 41006966 missense variant C/G;T snv 8.0E-06; 1.3E-04 0.010 1.000 1 2011 2011