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: rs2250635
rs2250635
4 15 41969267 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs4924590
rs4924590
3 15 41941475 intron variant T/A snv 0.30 0.700 1.000 1 2016 2016