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: rs2393732
rs2393732
2 0.925 0.120 10 62007470 intron variant G/A snv 0.15 0.010 < 0.001 1 2019 2019
dbSNP: rs4948488
rs4948488
2 0.925 0.120 10 61925395 intron variant C/A;T snv 0.010 < 0.001 1 2019 2019