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: rs174555
rs174555
4 11 61812288 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs61897795
rs61897795
3 11 61850697 intron variant A/G snv 9.5E-02 0.700 1.000 1 2016 2016