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: rs77972916
rs77972916
1 2 43534973 intron variant G/A snv 4.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs78487399
rs78487399
5 2 43582208 intron variant G/C snv 6.2E-02 0.700 1.000 1 2016 2016