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: rs16856859
rs16856859
2 3 172066946 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs35461662
rs35461662
2 3 172056222 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs6763687
rs6763687
2 3 172059856 intron variant A/G;T snv 0.700 1.000 1 2016 2016