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: rs279722
rs279722
1 1.000 0.040 20 46458571 intron variant G/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs279725
rs279725
1 1.000 0.040 20 46455349 non coding transcript exon variant T/C snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs4809590
rs4809590
1 1.000 0.040 20 46456188 non coding transcript exon variant G/A snv 0.18 0.700 1.000 1 2017 2017