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: rs1461677
rs1461677
1 11 99317151 intron variant T/G snv 0.94 0.700 1.000 1 2019 2019
dbSNP: rs2614546
rs2614546
1 11 99333522 intron variant T/C snv 6.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs4316475
rs4316475
1 11 99180791 intron variant G/A snv 0.94 0.700 1.000 1 2018 2018