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: rs3213801
rs3213801
3 0.882 0.080 5 75581441 synonymous variant C/T snv 0.24 0.22 0.010 < 0.001 1 2019 2019
dbSNP: rs5744533
rs5744533
6 0.807 0.120 5 75510279 intron variant C/A;T snv 0.010 < 0.001 1 2019 2019