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: rs6432622
rs6432622
1 2 160483759 intron variant A/G snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs7424771
rs7424771
4 2 160419867 intron variant G/A snv 0.44 0.700 1.000 1 2019 2019