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: rs543267101
rs543267101
1 1.000 6 44300612 missense variant C/T snv 4.0E-05 4.2E-05 0.800 1.000 1 2014 2014
dbSNP: rs587777590
rs587777590
1 1.000 6 44313175 missense variant A/C snv 0.800 1.000 1 2014 2014
dbSNP: rs587777592
rs587777592
1 1.000 6 44306367 missense variant C/T snv 1.6E-05 7.0E-06 0.800 1.000 1 2014 2014