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: rs492602
rs492602
7 0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 0.700 1.000 2 2018 2019
dbSNP: rs516246
rs516246
10 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2018 2018
dbSNP: rs679574
rs679574
7 0.827 0.120 19 48702851 intron variant C/G snv 0.45 0.700 1.000 1 2018 2018