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: rs1065411
rs1065411
2 0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06 0.010 1.000 1 2010 2010
dbSNP: rs768623239
rs768623239
26 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 0.010 1.000 1 2015 2015