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: rs12935413
rs12935413
3 1.000 0.080 16 11116590 intron variant G/A snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs62026377
rs62026377
1 16 11135271 intron variant G/T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs8061043
rs8061043
1 16 11067072 intron variant G/T snv 0.19 0.700 1.000 1 2019 2019