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: rs1991866
rs1991866
3 8 129611859 intron variant G/A;C snv 0.800 1.000 2 2012 2017
dbSNP: rs13277237
rs13277237
4 8 129592317 intron variant G/A snv 0.53 0.700 1.000 1 2015 2015