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: rs150283105
rs150283105
2 3 128909410 missense variant C/T snv 7.2E-05 1.3E-04 0.010 1.000 1 2017 2017
dbSNP: rs763004980
rs763004980
2 3 128906139 missense variant G/A snv 1.2E-05 1.4E-05 0.010 1.000 1 2017 2017