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: rs59811240
rs59811240
2 1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs75629841
rs75629841
2 1.000 0.080 8 124714135 intron variant G/A;T snv 0.700 1.000 1 2017 2017