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: rs35032408
rs35032408
2 0.925 0.080 16 11121567 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs35441874
rs35441874
3 0.882 0.120 16 11119164 intron variant T/A snv 0.19 0.700 1.000 1 2019 2019