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: rs17028615
rs17028615
4 1.000 0.080 4 99150767 intron variant A/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs5860563
rs5860563
3 1.000 0.080 4 99126006 intron variant -/A delins 0.700 1.000 1 2019 2019