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: rs171748
rs171748
2 1.000 0.040 5 61203304 intron variant A/G snv 0.60 0.800 1.000 2 2013 2017
dbSNP: rs4391122
rs4391122
2 1.000 0.040 5 61302716 intron variant A/G snv 0.60 0.700 1.000 5 2014 2019