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: rs1573643
rs1573643
5 15 90877743 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs2071410
rs2071410
7 0.882 0.160 15 90877710 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018