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: rs267939
rs267939
DAP
1 1.000 0.040 5 10752203 intron variant C/T snv 0.50 0.800 1.000 1 2011 2011
dbSNP: rs2930047
rs2930047
DAP
3 0.925 0.040 5 10695414 intron variant T/C snv 0.49 0.700 1.000 1 2015 2015
dbSNP: rs3776414
rs3776414
DAP
6 0.827 0.120 5 10689450 intron variant T/G snv 0.48 0.700 1.000 1 2016 2016