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: rs1694068
rs1694068
4 5 53987800 intron variant T/A snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs702634
rs702634
3 1.000 0.080 5 53975590 intron variant G/A snv 0.72 0.700 1.000 1 2016 2016