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: rs17514846
rs17514846
7 0.882 0.120 15 90873320 intron variant C/A;G snv 0.700 1.000 2 2016 2018
dbSNP: rs1573643
rs1573643
5 15 90877743 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018