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: rs653178
rs653178
41 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 2 2011 2016
dbSNP: rs7137828
rs7137828
15 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2018 2018