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: rs6808837
rs6808837
1 3 141499112 intron variant T/C snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs9819371
rs9819371
5 3 141487958 intron variant C/T snv 4.7E-02 0.700 1.000 1 2016 2016