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: rs10408163
rs10408163
6 19 47093845 non coding transcript exon variant T/C snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs2303108
rs2303108
3 19 47086638 intron variant T/C snv 0.63 0.700 1.000 1 2017 2017
dbSNP: rs3810291
rs3810291
9 19 47065746 3 prime UTR variant G/A snv 0.50 0.700 1.000 1 2017 2017