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: rs17011903
rs17011903
2 0.925 0.040 1 208086186 intron variant C/A snv 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs7516841
rs7516841
2 0.925 0.040 1 208119358 intron variant G/C snv 0.95 0.700 1.000 1 2018 2018