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: rs17021918
rs17021918
8 0.776 0.240 4 94641726 intron variant C/T snv 0.30 0.700 1.000 2 2009 2018
dbSNP: rs12500426
rs12500426
5 0.851 0.240 4 94593458 intron variant A/C snv 0.54 0.700 1.000 1 2009 2009