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: rs62117911
rs62117911
2 19 16131076 intron variant G/A snv 0.14 0.700 1.000 2 2016 2019
dbSNP: rs1043407
rs1043407
1 19 16133416 3 prime UTR variant G/A;T snv 0.700 1.000 1 2018 2018