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: rs11066280
rs11066280
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs4766898
rs4766898
1 12 112344040 intron variant C/T snv 4.8E-02 0.700 1.000 1 2019 2019