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: rs58431213
rs58431213
1 15 92030832 intron variant G/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs7498044
rs7498044
1 15 92030409 intron variant G/A;T snv 0.700 1.000 1 2019 2019