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: rs4640244
rs4640244
3 17 21380911 intron variant A/G snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs7213608
rs7213608
2 17 21375977 upstream gene variant C/T snv 0.71 0.700 1.000 1 2019 2019