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: rs116990752
rs116990752
1 6 135589773 intron variant A/C;G snv 9.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs4895455
rs4895455
1 6 135746878 intron variant A/G snv 6.1E-02 0.700 1.000 1 2019 2019