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: rs1076560
rs1076560
11 0.776 0.120 11 113412966 intron variant C/A snv 0.16 0.020 1.000 2 2011 2014
dbSNP: rs1500
rs1500
2 1.000 0.080 5 76981013 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2020 2020
dbSNP: rs2283265
rs2283265
12 0.776 0.160 11 113414814 intron variant C/A snv 0.16 0.010 1.000 1 2011 2011