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: rs1106766
rs1106766
7 0.882 0.120 12 57415673 intron variant C/T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs12313306
rs12313306
2 12 57358071 intron variant C/T snv 0.19 0.700 1.000 1 2019 2019