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: rs12520745
rs12520745
1 1.000 0.120 5 125252697 intron variant C/T snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs17152484
rs17152484
1 1.000 0.120 5 125252465 intron variant C/A;G snv 0.700 1.000 1 2014 2014