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: rs313732
rs313732
1 1 85792920 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs313741
rs313741
1 1 85807768 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs380654
rs380654
1 1 85798342 intron variant C/G snv 0.33 0.700 1.000 1 2018 2018