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: rs4276643
rs4276643
2 8 27946082 intron variant C/T snv 0.64 0.700 1.000 2 2016 2019
dbSNP: rs62496810
rs62496810
1 8 27957964 intron variant C/T snv 2.7E-02 0.700 1.000 1 2019 2019