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: rs1122608
rs1122608
16 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1529729
rs1529729
3 19 11052886 intron variant C/T snv 0.58 0.700 1.000 1 2012 2012