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: rs3136441
rs3136441
F2
1 11 46721697 intron variant T/C snv 0.13 0.800 1.000 4 2010 2019
dbSNP: rs75185853
rs75185853
F2
1 11 46729851 intron variant T/C snv 0.700 1.000 1 2018 2018