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: rs4727695
rs4727695
1 7 107973558 intron variant A/G snv 8.3E-02 0.700 1.000 2 2018 2019
dbSNP: rs11760290
rs11760290
1 7 107975623 intron variant T/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs76335902
rs76335902
1 7 107969061 intron variant A/C;G snv 0.700 1.000 1 2019 2019