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: rs4810485
rs4810485
4 0.732 0.480 20 46119308 intron variant T/A;G snv 0.840 1.000 3 2008 2016
dbSNP: rs4239702
rs4239702
1 1.000 0.120 20 46120612 intron variant T/C snv 0.75 0.800 1.000 1 2014 2019